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AACTGTTGTATGTATGGATTGCTTT[C/T]GTGAGAGTTTTTACATTTTTGAAAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602040 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NCAM2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
|
NCAM2 - neural cell adhesion molecule 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004540.3 | Intron | NP_004531.2 | ||||
XM_011529575.2 | Intron | XP_011527877.1 | ||||
XM_011529576.2 | Intron | XP_011527878.1 | ||||
XM_011529579.2 | Intron | XP_011527881.1 | ||||
XM_011529580.2 | Intron | XP_011527882.1 | ||||
XM_011529581.2 | Intron | XP_011527883.1 | ||||
XM_011529582.2 | Intron | XP_011527884.1 | ||||
XM_011529585.2 | Intron | XP_011527887.1 | ||||
XM_017028353.1 | Intron | XP_016883842.1 | ||||
XM_017028354.1 | Intron | XP_016883843.1 | ||||
XM_017028355.1 | Intron | XP_016883844.1 | ||||
XM_017028356.1 | Intron | XP_016883845.1 | ||||
XM_017028357.1 | Intron | XP_016883846.1 | ||||
XM_017028358.1 | Intron | XP_016883847.1 |