Canonical Allele Identifier: CA363311171

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31355527-C-A
• gnomAD v4: 6-31355527-C-A
• MyVariant Identifiers: chr6:g.31323304C>A (hg19) ; chr6:g.31355527C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355527C>A , CM000668.2:g.31355527C>A	GRCh38
NC_000006.11:g.31323304C>A , CM000668.1:g.31323304C>A	GRCh37
NC_000006.10:g.31431283C>A	NCBI36
NG_023187.1:g.6686G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2732G>T
ENST00000481849.6:n.2158G>T
ENST00000497377.6:n.2158G>T
ENST00000640094.2:c.685G>T	ENSP00000491275.2:p.Ala229Ser
ENST00000696558.1:c.754G>T	ENSP00000512716.1:n.754G>T
ENST00000696559.1:c.685G>T	ENSP00000512717.1:p.Ala229Ser
ENST00000696560.1:c.685G>T	ENSP00000512718.1:p.Ala229Ser
ENST00000696561.1:c.685G>T	ENSP00000512719.1:p.Ala229Ser
ENST00000696562.1:c.685G>T	ENSP00000512720.1:p.Ala229Ser
ENST00000412585.7:c.685G>T MANE Select	ENSP00000399168.2:p.Ala229Ser
ENST00000412585.6:c.685G>T	ENSP00000399168.2:p.Ala229Ser
ENST00000434333.1:c.718G>T	ENSP00000405931.1:p.Ala240Ser
ENST00000463574.1:n.276G>T
ENST00000474381.1:n.1134G>T
ENST00000498007.1:n.951G>T
NM_005514.6:c.685G>T	NP_005505.2:p.Ala229Ser
XM_011514556.1:c.718G>T	XP_011512858.1:p.Ala240Ser
XM_011514557.1:c.685G>T	XP_011512859.1:p.Ala229Ser
XR_926175.1:n.1124G>T
NM_005514.7:c.685G>T	NP_005505.2:p.Ala229Ser
NM_005514.8:c.685G>T MANE Select	NP_005505.2:p.Ala229Ser