Canonical Allele Identifier: CA136833614

Gene: HLA-B

Linked Data

• dbSNP Id: rs151341327
• gnomAD v3: 6-31356194-T-C
• gnomAD v4: 6-31356194-T-C
• MyVariant Identifiers: chr6:g.31323971T>C (hg19) ; chr6:g.31356194T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356194T>C , CM000668.2:g.31356194T>C	GRCh38
NC_000006.11:g.31323971T>C , CM000668.1:g.31323971T>C	GRCh37
NC_000006.10:g.31431950T>C	NCBI36
NG_023187.1:g.6019A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2065A>G
ENST00000481849.6:n.2065A>G
ENST00000497377.6:n.2065A>G
ENST00000640094.2:c.592A>G	ENSP00000491275.2:p.Asn198Asp
ENST00000696558.1:c.592A>G	ENSP00000512716.1:p.Asn198Asp
ENST00000696559.1:c.592A>G	ENSP00000512717.1:p.Asn198Asp
ENST00000696560.1:c.592A>G	ENSP00000512718.1:p.Asn198Asp
ENST00000696561.1:c.592A>G	ENSP00000512719.1:p.Asn198Asp
ENST00000696562.1:c.592A>G	ENSP00000512720.1:p.Asn198Asp
ENST00000412585.7:c.592A>G MANE Select	ENSP00000399168.2:p.Asn198Asp
ENST00000412585.6:c.592A>G	ENSP00000399168.2:p.Asn198Asp
ENST00000434333.1:c.625A>G	ENSP00000405931.1:p.Asn209Asp
ENST00000474381.1:n.467A>G
ENST00000498007.1:n.858A>G
NM_005514.6:c.592A>G	NP_005505.2:p.Asn198Asp
XM_011514556.1:c.625A>G	XP_011512858.1:p.Asn209Asp
XM_011514557.1:c.592A>G	XP_011512859.1:p.Asn198Asp
XR_926175.1:n.602A>G
NM_005514.7:c.592A>G	NP_005505.2:p.Asn198Asp
NM_005514.8:c.592A>G MANE Select	NP_005505.2:p.Asn198Asp