Canonical Allele Identifier: CA363308601

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355136-G-A
• MyVariant Identifiers: chr6:g.31322913G>A (hg19) ; chr6:g.31355136G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355136G>A , CM000668.2:g.31355136G>A	GRCh38
NC_000006.11:g.31322913G>A , CM000668.1:g.31322913G>A	GRCh37
NC_000006.10:g.31430892G>A	NCBI36
NG_023187.1:g.7077C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3030C>T
ENST00000481849.6:n.2549C>T
ENST00000497377.6:n.2456C>T
ENST00000640094.2:c.895+181C>T	ENSP00000491275.2:n.895+181C>T
ENST00000696558.1:c.1052C>T	ENSP00000512716.1:n.1052C>T
ENST00000696559.1:c.983C>T	ENSP00000512717.1:p.Ala328Val
ENST00000696560.1:c.983C>T	ENSP00000512718.1:p.Ala328Val
ENST00000696561.1:c.983C>T	ENSP00000512719.1:p.Ala328Val
ENST00000696562.1:c.983C>T	ENSP00000512720.1:p.Ala328Val
ENST00000412585.7:c.983C>T MANE Select	ENSP00000399168.2:p.Ala328Val
ENST00000640094.1:c.88+181C>T	ENSP00000491275.1:n.88+181C>T
ENST00000412585.6:c.983C>T	ENSP00000399168.2:p.Ala328Val
ENST00000463574.1:n.574C>T
NM_005514.6:c.983C>T	NP_005505.2:p.Ala328Val
XM_011514556.1:c.1016C>T	XP_011512858.1:p.Ala339Val
XM_011514557.1:c.895+181C>T	XP_011512859.1:n.895+181C>T
XR_926175.1:n.1422C>T
NM_005514.7:c.983C>T	NP_005505.2:p.Ala328Val
NM_005514.8:c.983C>T MANE Select	NP_005505.2:p.Ala328Val