Canonical Allele Identifier: CA363307833

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354487-G-A
• MyVariant Identifiers: chr6:g.31322264G>A (hg19) ; chr6:g.31354487G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354487G>A , CM000668.2:g.31354487G>A	GRCh38
NC_000006.11:g.31322264G>A , CM000668.1:g.31322264G>A	GRCh37
NC_000006.10:g.31430243G>A	NCBI36
NG_023187.1:g.7726C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3132C>T
ENST00000481849.6:n.3092C>T
ENST00000497377.6:n.2999C>T
ENST00000640094.2:c.968C>T	ENSP00000491275.2:p.Ala323Val
ENST00000696558.1:c.1154C>T	ENSP00000512716.1:n.1154C>T
ENST00000696559.1:c.1085C>T	ENSP00000512717.1:p.Ala362Val
ENST00000696560.1:c.1085C>T	ENSP00000512718.1:p.Ala362Val
ENST00000696561.1:c.1085C>T	ENSP00000512719.1:p.Ala362Val
ENST00000696562.1:c.1085C>T	ENSP00000512720.1:p.Ala362Val
ENST00000412585.7:c.1085C>T MANE Select	ENSP00000399168.2:p.Ala362Val
ENST00000412585.6:c.1085C>T	ENSP00000399168.2:p.Ala362Val
ENST00000481849.5:n.320C>T
ENST00000497377.5:n.484C>T
NM_005514.6:c.1085C>T	NP_005505.2:p.Ala362Val
XM_011514556.1:c.1118C>T	XP_011512858.1:p.Ala373Val
XM_011514557.1:c.968C>T	XP_011512859.1:p.Ala323Val
XR_926175.1:n.1524C>T
NM_005514.7:c.1085C>T	NP_005505.2:p.Ala362Val
NM_005514.8:c.1085C>T MANE Select	NP_005505.2:p.Ala362Val