Canonical Allele Identifier: CA2677954359

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354651-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354654del , CM000668.2:g.31354654del	GRCh38
NC_000006.11:g.31322431del , CM000668.1:g.31322431del	GRCh37
NC_000006.10:g.31430410del	NCBI36
NG_023187.1:g.7561del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3073del
ENST00000481849.6:n.3033del
ENST00000497377.6:n.2940del
ENST00000640094.2:c.909del	ENSP00000491275.2:p.Ser304AlafsTer?
ENST00000696558.1:c.1095del	ENSP00000512716.1:n.1095del
ENST00000696559.1:c.1026del	ENSP00000512717.1:p.Ser343AlafsTer29
ENST00000696560.1:c.1026del	ENSP00000512718.1:p.Ser343AlafsTer29
ENST00000696561.1:c.1026del	ENSP00000512719.1:p.Ser343AlafsTer29
ENST00000696562.1:c.1026del	ENSP00000512720.1:p.Ser343AlafsTer29
ENST00000412585.7:c.1026del MANE Select	ENSP00000399168.2:p.Ser343AlafsTer29
ENST00000640094.1:c.102del	ENSP00000491275.1:p.Ser35AlafsTer?
ENST00000412585.6:c.1026del	ENSP00000399168.2:p.Ser343AlafsTer29
ENST00000481849.5:n.155del
ENST00000497377.5:n.425del
NM_005514.6:c.1026del	NP_005505.2:p.Ser343AlafsTer29
XM_011514556.1:c.1059del	XP_011512858.1:p.Ser354AlafsTer29
XM_011514557.1:c.909del	XP_011512859.1:p.Ser304AlafsTer29
XR_926175.1:n.1465del
NM_005514.7:c.1026del	NP_005505.2:p.Ser343AlafsTer29
NM_005514.8:c.1026del MANE Select	NP_005505.2:p.Ser343AlafsTer29