Canonical Allele Identifier: CA1619119592

Gene: HLA-B

Linked Data

• dbSNP Id: rs1766905545

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355860_31355861del , CM000668.2:g.31355860_31355861del	GRCh38
NC_000006.11:g.31323637_31323638del , CM000668.1:g.31323637_31323638del	GRCh37
NC_000006.10:g.31431616_31431617del	NCBI36
NG_023187.1:g.6352_6353del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2398_2399del
ENST00000481849.6:n.2093-269_2093-268del
ENST00000497377.6:n.2093-269_2093-268del
ENST00000640094.2:c.620-269_620-268del	ENSP00000491275.2:n.620-269_620-268del
ENST00000696558.1:c.620-55_620-54del	ENSP00000512716.1:n.620-55_620-54del
ENST00000696559.1:c.620-269_620-268del	ENSP00000512717.1:n.620-269_620-268del
ENST00000696560.1:c.620-269_620-268del	ENSP00000512718.1:n.620-269_620-268del
ENST00000696561.1:c.620-269_620-268del	ENSP00000512719.1:n.620-269_620-268del
ENST00000696562.1:c.620-269_620-268del	ENSP00000512720.1:n.620-269_620-268del
ENST00000412585.7:c.620-269_620-268del MANE Select	ENSP00000399168.2:n.620-269_620-268del
ENST00000412585.6:c.620-269_620-268del	ENSP00000399168.2:n.620-269_620-268del
ENST00000434333.1:c.653-269_653-268del	ENSP00000405931.1:n.653-269_653-268del
ENST00000474381.1:n.800_801del
ENST00000498007.1:n.886-269_886-268del
NM_005514.6:c.620-269_620-268del	NP_005505.2:n.620-269_620-268del
XM_011514556.1:c.653-269_653-268del	XP_011512858.1:n.653-269_653-268del
XM_011514557.1:c.620-269_620-268del	XP_011512859.1:n.620-269_620-268del
XR_926175.1:n.935_936del
NM_005514.7:c.620-269_620-268del	NP_005505.2:n.620-269_620-268del
NM_005514.8:c.620-269_620-268del MANE Select	NP_005505.2:n.620-269_620-268del