Canonical Allele Identifier: CA363307841

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354488-C-T
• MyVariant Identifiers: chr6:g.31322265C>T (hg19) ; chr6:g.31354488C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354488C>T , CM000668.2:g.31354488C>T	GRCh38
NC_000006.11:g.31322265C>T , CM000668.1:g.31322265C>T	GRCh37
NC_000006.10:g.31430244C>T	NCBI36
NG_023187.1:g.7725G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3131G>A
ENST00000481849.6:n.3091G>A
ENST00000497377.6:n.2998G>A
ENST00000640094.2:c.967G>A	ENSP00000491275.2:p.Ala323Thr
ENST00000696558.1:c.1153G>A	ENSP00000512716.1:n.1153G>A
ENST00000696559.1:c.1084G>A	ENSP00000512717.1:p.Ala362Thr
ENST00000696560.1:c.1084G>A	ENSP00000512718.1:p.Ala362Thr
ENST00000696561.1:c.1084G>A	ENSP00000512719.1:p.Ala362Thr
ENST00000696562.1:c.1084G>A	ENSP00000512720.1:p.Ala362Thr
ENST00000412585.7:c.1084G>A MANE Select	ENSP00000399168.2:p.Ala362Thr
ENST00000412585.6:c.1084G>A	ENSP00000399168.2:p.Ala362Thr
ENST00000481849.5:n.319G>A
ENST00000497377.5:n.483G>A
NM_005514.6:c.1084G>A	NP_005505.2:p.Ala362Thr
XM_011514556.1:c.1117G>A	XP_011512858.1:p.Ala373Thr
XM_011514557.1:c.967G>A	XP_011512859.1:p.Ala323Thr
XR_926175.1:n.1523G>A
NM_005514.7:c.1084G>A	NP_005505.2:p.Ala362Thr
NM_005514.8:c.1084G>A MANE Select	NP_005505.2:p.Ala362Thr