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ATGGGTGGTCGGCCTCCTGCCCTTC[C/G]ATGGCATCCCTTGCTTGGAGCACTG
Species: |
Human | ||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607904 | ||||||||||||||||||||||||||||||||
Literature Links: |
CACNA1H PubMed Links | ||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global - Not Available | Caucasian
|
CEPH (CEU) - Not Available | |||
EAS - Not Available | African American
|
YRI (Yoruba) - Not Available | |||
SAS - Not Available | Japanese
|
CHB (Han Chinese) - Not Available | |||
AFR - Not Available | Chinese
|
JPT (Japanese) - Not Available | |||
EUR - Not Available | |||||
AMR - Not Available |
CACNA1H - calcium voltage-gated channel subunit alpha1 H | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001005407.1 | Intron | NP_001005407.1 | ||||
NM_021098.2 | Intron | NP_066921.2 | ||||
XM_005255652.4 | Intron | XP_005255709.1 | ||||
XM_006720963.3 | Intron | XP_006721026.1 | ||||
XM_006720964.3 | Intron | XP_006721027.1 | ||||
XM_006720965.3 | Intron | XP_006721028.1 | ||||
XM_006720967.3 | Intron | XP_006721030.1 | ||||
XM_006720968.3 | Intron | XP_006721031.1 | ||||
XM_011522724.2 | Intron | XP_011521026.1 | ||||
XM_011522727.2 | Intron | XP_011521029.1 | ||||
XM_017023819.1 | Intron | XP_016879308.1 | ||||
XM_017023820.1 | Intron | XP_016879309.1 | ||||
XM_017023821.1 | Intron | XP_016879310.1 |
Set Membership: |
Validated |