Canonical Allele Identifier: CA136836502

Gene: HLA-B

Linked Data

• dbSNP Id: rs41556015
• gnomAD v3: 6-31356755-C-T
• gnomAD v4: 6-31356755-C-T
• MyVariant Identifiers: chr6:g.31324532C>T (hg19) ; chr6:g.31356755C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356755C>T , CM000668.2:g.31356755C>T	GRCh38
NC_000006.11:g.31324532C>T , CM000668.1:g.31324532C>T	GRCh37
NC_000006.10:g.31432511C>T	NCBI36
NG_023187.1:g.5458G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1749G>A
ENST00000481849.6:n.1749G>A
ENST00000497377.6:n.1749G>A
ENST00000640094.2:c.276G>A	ENSP00000491275.2:p.Lys92=
ENST00000696558.1:c.276G>A	ENSP00000512716.1:p.Lys92=
ENST00000696559.1:c.276G>A	ENSP00000512717.1:p.Lys92=
ENST00000696560.1:c.276G>A	ENSP00000512718.1:p.Lys92=
ENST00000696561.1:c.276G>A	ENSP00000512719.1:p.Lys92=
ENST00000696562.1:c.276G>A	ENSP00000512720.1:p.Lys92=
ENST00000412585.7:c.276G>A MANE Select	ENSP00000399168.2:p.Lys92=
ENST00000412585.6:c.276G>A	ENSP00000399168.2:p.Lys92=
ENST00000434333.1:c.309G>A	ENSP00000405931.1:p.Lys103=
ENST00000474381.1:n.151G>A
ENST00000498007.1:n.297G>A
ENST00000603274.1:n.109C>T
NM_005514.6:c.276G>A	NP_005505.2:p.Lys92=
XM_011514556.1:c.309G>A	XP_011512858.1:p.Lys103=
XM_011514557.1:c.276G>A	XP_011512859.1:p.Lys92=
XR_926175.1:n.286G>A
NM_005514.7:c.276G>A	NP_005505.2:p.Lys92=
NM_005514.8:c.276G>A MANE Select	NP_005505.2:p.Lys92=