Canonical Allele Identifier: CA363312458

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31356265-G-T
• gnomAD v4: 6-31356265-G-T
• MyVariant Identifiers: chr6:g.31324042G>T (hg19) ; chr6:g.31356265G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356265G>T , CM000668.2:g.31356265G>T	GRCh38
NC_000006.11:g.31324042G>T , CM000668.1:g.31324042G>T	GRCh37
NC_000006.10:g.31432021G>T	NCBI36
NG_023187.1:g.5948C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1994C>A
ENST00000481849.6:n.1994C>A
ENST00000497377.6:n.1994C>A
ENST00000640094.2:c.521C>A	ENSP00000491275.2:p.Ala174Asp
ENST00000696558.1:c.521C>A	ENSP00000512716.1:p.Ala174Asp
ENST00000696559.1:c.521C>A	ENSP00000512717.1:p.Ala174Asp
ENST00000696560.1:c.521C>A	ENSP00000512718.1:p.Ala174Asp
ENST00000696561.1:c.521C>A	ENSP00000512719.1:p.Ala174Asp
ENST00000696562.1:c.521C>A	ENSP00000512720.1:p.Ala174Asp
ENST00000412585.7:c.521C>A MANE Select	ENSP00000399168.2:p.Ala174Asp
ENST00000412585.6:c.521C>A	ENSP00000399168.2:p.Ala174Asp
ENST00000434333.1:c.554C>A	ENSP00000405931.1:p.Ala185Asp
ENST00000474381.1:n.396C>A
ENST00000498007.1:n.787C>A
NM_005514.6:c.521C>A	NP_005505.2:p.Ala174Asp
XM_011514556.1:c.554C>A	XP_011512858.1:p.Ala185Asp
XM_011514557.1:c.521C>A	XP_011512859.1:p.Ala174Asp
XR_926175.1:n.531C>A
NM_005514.7:c.521C>A	NP_005505.2:p.Ala174Asp
NM_005514.8:c.521C>A MANE Select	NP_005505.2:p.Ala174Asp