Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATCGTTCCAATAATACCAGCCATCA[A/C]ACACAAAATAATGAGTATTATCACT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 111740 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GYPB PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
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
|
|||||
AMR
|
GYPB - glycophorin B (MNS blood group) | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001304382.1 | 266 | Missense Mutation | GTG,TTG | V,L 44 | NP_001291311.1 | |
NM_002100.5 | 266 | Missense Mutation | GTG,TTG | V,L 70 | NP_002091.3 | |
XM_011531903.2 | 266 | Missense Mutation | GTG,TTG | V,L 70 | XP_011530205.1 | |
XM_011531904.2 | 266 | Intron | XP_011530206.1 | |||
XM_011531905.2 | 266 | Missense Mutation | GTG,TTG | V,L 61 | XP_011530207.1 | |
XM_017008137.1 | 266 | Missense Mutation | GTG,TTG | V,L 44 | XP_016863626.1 |