Canonical Allele Identifier: CA3711800
Gene: HLA-B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1050570

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356772T>C , CM000668.2:g.31356772T>C GRCh38
NC_000006.11:g.31324549T>C , CM000668.1:g.31324549T>C GRCh37
NC_000006.10:g.31432528T>C NCBI36
NG_023187.1:g.5441A>G

Transcript Alleles

HGVS Amino-acid change
NM_005514.6:c.259A>G VV NP_005505.2:p.Asn87Asp
XM_011514556.1:c.292A>G XP_011512858.1:p.Asn98Asp
XM_011514557.1:c.259A>G XP_011512859.1:p.Asn87Asp
XR_926175.1:n.269A>G
NM_005514.7:c.259A>G VV
ENST00000412585.6:c.259A>G ENSP00000399168.2:p.Asn87Asp
ENST00000434333.1:c.292A>G ENSP00000405931.1:p.Asn98Asp
ENST00000474381.1:n.134A>G
ENST00000498007.1:n.280A>G
ENST00000603274.1:n.126T>C