Canonical Allele Identifier: CA2677954920

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355108-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355109del , CM000668.2:g.31355109del	GRCh38
NC_000006.11:g.31322886del , CM000668.1:g.31322886del	GRCh37
NC_000006.10:g.31430865del	NCBI36
NG_023187.1:g.7104del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3057del
ENST00000481849.6:n.2576del
ENST00000497377.6:n.2483del
ENST00000640094.2:c.895+208del	ENSP00000491275.2:n.895+208del
ENST00000696558.1:c.1079del	ENSP00000512716.1:n.1079del
ENST00000696559.1:c.1010del	ENSP00000512717.1:p.Ser337Ter
ENST00000696560.1:c.1010del	ENSP00000512718.1:p.Ser337Ter
ENST00000696561.1:c.1010del	ENSP00000512719.1:p.Ser337Ter
ENST00000696562.1:c.1010del	ENSP00000512720.1:p.Ser337Ter
ENST00000412585.7:c.1010del MANE Select	ENSP00000399168.2:p.Ser337Ter
ENST00000640094.1:c.88+208del	ENSP00000491275.1:n.88+208del
ENST00000412585.6:c.1010del	ENSP00000399168.2:p.Ser337Ter
NM_005514.6:c.1010del	NP_005505.2:p.Ser337Ter
XM_011514556.1:c.1043del	XP_011512858.1:p.Ser348Ter
XM_011514557.1:c.895+208del	XP_011512859.1:n.895+208del
XR_926175.1:n.1449del
NM_005514.7:c.1010del	NP_005505.2:p.Ser337Ter
NM_005514.8:c.1010del MANE Select	NP_005505.2:p.Ser337Ter