Canonical Allele Identifier: CA3711866
Gene: HLA-B HGNC NCBI

Linked Data

ClinVar Variation Id: 3055591
ClinVar RCV Id: RCV003972149
dbSNP Id: rs9266183
gnomAD v2: 6-31324647-T-C
gnomAD v3: 6-31356870-T-C
gnomAD v4: 6-31356870-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356870T>C , CM000668.2:g.31356870T>C GRCh38
NC_000006.11:g.31324647T>C , CM000668.1:g.31324647T>C GRCh37
NC_000006.10:g.31432626T>C NCBI36
NG_023187.1:g.5343A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1634A>G
ENST00000481849.6:n.1634A>G
ENST00000497377.6:n.1634A>G
ENST00000640094.2:c.161A>G ENSP00000491275.2:p.Asp54Gly
ENST00000696558.1:c.161A>G ENSP00000512716.1:p.Asp54Gly
ENST00000696559.1:c.161A>G ENSP00000512717.1:p.Asp54Gly
ENST00000696560.1:c.161A>G ENSP00000512718.1:p.Asp54Gly
ENST00000696561.1:c.161A>G ENSP00000512719.1:p.Asp54Gly
ENST00000696562.1:c.161A>G ENSP00000512720.1:p.Asp54Gly
ENST00000412585.7:c.161A>G MANE Select ENSP00000399168.2:p.Asp54Gly
ENST00000412585.6:c.161A>G ENSP00000399168.2:p.Asp54Gly
ENST00000434333.1:c.194A>G ENSP00000405931.1:p.Asp65Gly
ENST00000474381.1:n.36A>G
ENST00000498007.1:n.182A>G
ENST00000603274.1:n.224T>C
NM_005514.6:c.161A>G NP_005505.2:p.Asp54Gly
XM_011514556.1:c.194A>G XP_011512858.1:p.Asp65Gly
XM_011514557.1:c.161A>G XP_011512859.1:p.Asp54Gly
XR_926175.1:n.171A>G
NM_005514.7:c.161A>G NP_005505.2:p.Asp54Gly
NM_005514.8:c.161A>G MANE Select NP_005505.2:p.Asp54Gly