Canonical Allele Identifier: CA449599598

Gene: HLA-B

Linked Data

• dbSNP Id: rs1766747807
• gnomAD v3: 6-31354646-G-A
• gnomAD v4: 6-31354646-G-A
• MyVariant Identifiers: chr6:g.31322423G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354646G>A , CM000668.2:g.31354646G>A	GRCh38
NC_000006.11:g.31322423G>A , CM000668.1:g.31322423G>A	GRCh37
NC_000006.10:g.31430402G>A	NCBI36
NG_023187.1:g.7567C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3079C>T
ENST00000481849.6:n.3039C>T
ENST00000497377.6:n.2946C>T
ENST00000640094.2:c.915C>T	ENSP00000491275.2:p.Tyr305=
ENST00000696558.1:c.1101C>T	ENSP00000512716.1:n.1101C>T
ENST00000696559.1:c.1032C>T	ENSP00000512717.1:p.Tyr344=
ENST00000696560.1:c.1032C>T	ENSP00000512718.1:p.Tyr344=
ENST00000696561.1:c.1032C>T	ENSP00000512719.1:p.Tyr344=
ENST00000696562.1:c.1032C>T	ENSP00000512720.1:p.Tyr344=
ENST00000412585.7:c.1032C>T MANE Select	ENSP00000399168.2:p.Tyr344=
ENST00000640094.1:c.108C>T	ENSP00000491275.1:p.Tyr36=
ENST00000412585.6:c.1032C>T	ENSP00000399168.2:p.Tyr344=
ENST00000481849.5:n.161C>T
ENST00000497377.5:n.431C>T
NM_005514.6:c.1032C>T	NP_005505.2:p.Tyr344=
XM_011514556.1:c.1065C>T	XP_011512858.1:p.Tyr355=
XM_011514557.1:c.915C>T	XP_011512859.1:p.Tyr305=
XR_926175.1:n.1471C>T
NM_005514.7:c.1032C>T	NP_005505.2:p.Tyr344=
NM_005514.8:c.1032C>T MANE Select	NP_005505.2:p.Tyr344=