Canonical Allele Identifier: CA1619112519

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356609_31356610delinsAC , CM000668.2:g.31356609_31356610delinsAC	GRCh38
NC_000006.11:g.31324386_31324387delinsAC , CM000668.1:g.31324386_31324387delinsAC	GRCh37
NC_000006.10:g.31432365_31432366delinsAC	NCBI36
NG_023187.1:g.5603_5604delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1816+78_1816+79delinsGT
ENST00000481849.6:n.1816+78_1816+79delinsGT
ENST00000497377.6:n.1816+78_1816+79delinsGT
ENST00000640094.2:c.343+78_343+79delinsGT	ENSP00000491275.2:n.343+78_343+79delinsGT
ENST00000696558.1:c.343+78_343+79delinsGT	ENSP00000512716.1:n.343+78_343+79delinsGT
ENST00000696559.1:c.343+78_343+79delinsGT	ENSP00000512717.1:n.343+78_343+79delinsGT
ENST00000696560.1:c.343+78_343+79delinsGT	ENSP00000512718.1:n.343+78_343+79delinsGT
ENST00000696561.1:c.343+78_343+79delinsGT	ENSP00000512719.1:n.343+78_343+79delinsGT
ENST00000696562.1:c.343+78_343+79delinsGT	ENSP00000512720.1:n.343+78_343+79delinsGT
ENST00000412585.7:c.343+78_343+79delinsGT MANE Select	ENSP00000399168.2:n.343+78_343+79delinsGT
ENST00000412585.6:c.343+78_343+79delinsGT	ENSP00000399168.2:n.343+78_343+79delinsGT
ENST00000434333.1:c.376+78_376+79delinsGT	ENSP00000405931.1:n.376+78_376+79delinsGT
ENST00000474381.1:n.218+78_218+79delinsGT
ENST00000498007.1:n.442_443delinsGT
NM_005514.6:c.343+78_343+79delinsGT	NP_005505.2:n.343+78_343+79delinsGT
XM_011514556.1:c.376+78_376+79delinsGT	XP_011512858.1:n.376+78_376+79delinsGT
XM_011514557.1:c.343+78_343+79delinsGT	XP_011512859.1:n.343+78_343+79delinsGT
XR_926175.1:n.353+78_353+79delinsGT
NM_005514.7:c.343+78_343+79delinsGT	NP_005505.2:n.343+78_343+79delinsGT
NM_005514.8:c.343+78_343+79delinsGT MANE Select	NP_005505.2:n.343+78_343+79delinsGT