Canonical Allele Identifier: CA3711895
Gene: HLA-B HGNC NCBI

Linked Data

ClinVar Variation Id: 3059738
ClinVar RCV Id: RCV003974709
dbSNP Id: rs2596492
gnomAD v2: 6-31324711-A-G
gnomAD v3: 6-31356934-A-G
gnomAD v4: 6-31356934-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356934A>G , CM000668.2:g.31356934A>G GRCh38
NC_000006.11:g.31324711A>G , CM000668.1:g.31324711A>G GRCh37
NC_000006.10:g.31432690A>G NCBI36
NG_023187.1:g.5279T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1570T>C
ENST00000481849.6:n.1570T>C
ENST00000497377.6:n.1570T>C
ENST00000640094.2:c.97T>C ENSP00000491275.2:p.Tyr33His
ENST00000696558.1:c.97T>C ENSP00000512716.1:p.Tyr33His
ENST00000696559.1:c.97T>C ENSP00000512717.1:p.Tyr33His
ENST00000696560.1:c.97T>C ENSP00000512718.1:p.Tyr33His
ENST00000696561.1:c.97T>C ENSP00000512719.1:p.Tyr33His
ENST00000696562.1:c.97T>C ENSP00000512720.1:p.Tyr33His
ENST00000412585.7:c.97T>C MANE Select ENSP00000399168.2:p.Tyr33His
ENST00000412585.6:c.97T>C ENSP00000399168.2:p.Tyr33His
ENST00000434333.1:c.130T>C ENSP00000405931.1:p.Tyr44His
ENST00000498007.1:n.118T>C
ENST00000603274.1:n.288A>G
NM_005514.6:c.97T>C NP_005505.2:p.Tyr33His
XM_011514556.1:c.130T>C XP_011512858.1:p.Tyr44His
XM_011514557.1:c.97T>C XP_011512859.1:p.Tyr33His
XR_926175.1:n.107T>C
NM_005514.7:c.97T>C NP_005505.2:p.Tyr33His
NM_005514.8:c.97T>C MANE Select NP_005505.2:p.Tyr33His