Canonical Allele Identifier: CA1619116337

Gene: HLA-B

Linked Data

• dbSNP Id: rs1766636982

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31353945del , CM000668.2:g.31353945del	GRCh38
NC_000006.11:g.31321722del , CM000668.1:g.31321722del	GRCh37
NC_000006.10:g.31429701del	NCBI36
NG_023187.1:g.8269del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3493del
ENST00000481849.6:n.3453del
ENST00000497377.6:n.3360del
ENST00000696558.1:c.1515del	ENSP00000512716.1:n.1515del
ENST00000696559.1:c.*357del	ENSP00000512717.1:n.*357del
ENST00000696560.1:c.*357del	ENSP00000512718.1:n.*357del
ENST00000696561.1:c.*357del	ENSP00000512719.1:n.*357del
ENST00000696562.1:c.*357del	ENSP00000512720.1:n.*357del
ENST00000412585.7:c.*357del MANE Select	ENSP00000399168.2:n.*357del
ENST00000412585.6:c.*357del	ENSP00000399168.2:n.*357del
ENST00000481849.5:n.681del
ENST00000497377.5:n.845del
NM_005514.6:c.*357del	NP_005505.2:n.*357del
XM_011514556.1:c.*357del	XP_011512858.1:n.*357del
XM_011514557.1:c.*357del	XP_011512859.1:n.*357del
XR_926175.1:n.1885del
NM_005514.7:c.*357del	NP_005505.2:n.*357del
NM_005514.8:c.*357del MANE Select	NP_005505.2:n.*357del