Canonical Allele Identifier: CA1619111699

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356308_31356309delinsCG , CM000668.2:g.31356308_31356309delinsCG	GRCh38
NC_000006.11:g.31324085_31324086delinsCG , CM000668.1:g.31324085_31324086delinsCG	GRCh37
NC_000006.10:g.31432064_31432065delinsCG	NCBI36
NG_023187.1:g.5904_5905delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1950_1951delinsCG
ENST00000481849.6:n.1950_1951delinsCG
ENST00000497377.6:n.1950_1951delinsCG
ENST00000640094.2:c.477_478delinsCG	ENSP00000491275.2:p.Ala159=
ENST00000696558.1:c.477_478delinsCG	ENSP00000512716.1:p.Ala159=
ENST00000696559.1:c.477_478delinsCG	ENSP00000512717.1:p.Ala159=
ENST00000696560.1:c.477_478delinsCG	ENSP00000512718.1:p.Ala159=
ENST00000696561.1:c.477_478delinsCG	ENSP00000512719.1:p.Ala159=
ENST00000696562.1:c.477_478delinsCG	ENSP00000512720.1:p.Ala159=
ENST00000412585.7:c.477_478delinsCG MANE Select	ENSP00000399168.2:p.Ala159=
ENST00000412585.6:c.477_478delinsCG	ENSP00000399168.2:p.Ala159=
ENST00000434333.1:c.510_511delinsCG	ENSP00000405931.1:p.Ala170=
ENST00000474381.1:n.352_353delinsCG
ENST00000498007.1:n.743_744delinsCG
NM_005514.6:c.477_478delinsCG	NP_005505.2:p.Ala159=
XM_011514556.1:c.510_511delinsCG	XP_011512858.1:p.Ala170=
XM_011514557.1:c.477_478delinsCG	XP_011512859.1:p.Ala159=
XR_926175.1:n.487_488delinsCG
NM_005514.7:c.477_478delinsCG	NP_005505.2:p.Ala159=
NM_005514.8:c.477_478delinsCG MANE Select	NP_005505.2:p.Ala159=