Canonical Allele Identifier: CA363311289

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355556-G-T
• MyVariant Identifiers: chr6:g.31323333G>T (hg19) ; chr6:g.31355556G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355556G>T , CM000668.2:g.31355556G>T	GRCh38
NC_000006.11:g.31323333G>T , CM000668.1:g.31323333G>T	GRCh37
NC_000006.10:g.31431312G>T	NCBI36
NG_023187.1:g.6657C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2703C>A
ENST00000481849.6:n.2129C>A
ENST00000497377.6:n.2129C>A
ENST00000640094.2:c.656C>A	ENSP00000491275.2:p.Ser219Tyr
ENST00000696558.1:c.725C>A	ENSP00000512716.1:n.725C>A
ENST00000696559.1:c.656C>A	ENSP00000512717.1:p.Ser219Tyr
ENST00000696560.1:c.656C>A	ENSP00000512718.1:p.Ser219Tyr
ENST00000696561.1:c.656C>A	ENSP00000512719.1:p.Ser219Tyr
ENST00000696562.1:c.656C>A	ENSP00000512720.1:p.Ser219Tyr
ENST00000412585.7:c.656C>A MANE Select	ENSP00000399168.2:p.Ser219Tyr
ENST00000412585.6:c.656C>A	ENSP00000399168.2:p.Ser219Tyr
ENST00000434333.1:c.689C>A	ENSP00000405931.1:p.Ser230Tyr
ENST00000463574.1:n.247C>A
ENST00000474381.1:n.1105C>A
ENST00000498007.1:n.922C>A
NM_005514.6:c.656C>A	NP_005505.2:p.Ser219Tyr
XM_011514556.1:c.689C>A	XP_011512858.1:p.Ser230Tyr
XM_011514557.1:c.656C>A	XP_011512859.1:p.Ser219Tyr
XR_926175.1:n.1095C>A
NM_005514.7:c.656C>A	NP_005505.2:p.Ser219Tyr
NM_005514.8:c.656C>A MANE Select	NP_005505.2:p.Ser219Tyr