Canonical Allele Identifier: CA1619118179

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355133_31355134delinsGC , CM000668.2:g.31355133_31355134delinsGC	GRCh38
NC_000006.11:g.31322910_31322911delinsGC , CM000668.1:g.31322910_31322911delinsGC	GRCh37
NC_000006.10:g.31430889_31430890delinsGC	NCBI36
NG_023187.1:g.7079_7080delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3032_3033delinsGC
ENST00000481849.6:n.2551_2552delinsGC
ENST00000497377.6:n.2458_2459delinsGC
ENST00000640094.2:c.895+183_895+184delinsGC	ENSP00000491275.2:n.895+183_895+184delins...
ENST00000696558.1:c.1054_1055delinsGC	ENSP00000512716.1:n.1054_1055delinsGC
ENST00000696559.1:c.985_986delinsGC	ENSP00000512717.1:p.Ala329=
ENST00000696560.1:c.985_986delinsGC	ENSP00000512718.1:p.Ala329=
ENST00000696561.1:c.985_986delinsGC	ENSP00000512719.1:p.Ala329=
ENST00000696562.1:c.985_986delinsGC	ENSP00000512720.1:p.Ala329=
ENST00000412585.7:c.985_986delinsGC MANE Select	ENSP00000399168.2:p.Ala329=
ENST00000640094.1:c.88+183_88+184delinsGC	ENSP00000491275.1:n.88+183_88+184delinsGC...
ENST00000412585.6:c.985_986delinsGC	ENSP00000399168.2:p.Ala329=
ENST00000463574.1:n.576_577delinsGC
NM_005514.6:c.985_986delinsGC	NP_005505.2:p.Ala329=
XM_011514556.1:c.1018_1019delinsGC	XP_011512858.1:p.Ala340=
XM_011514557.1:c.895+183_895+184delinsGC	XP_011512859.1:n.895+183_895+184delinsGC
XR_926175.1:n.1424_1425delinsGC
NM_005514.7:c.985_986delinsGC	NP_005505.2:p.Ala329=
NM_005514.8:c.985_986delinsGC MANE Select	NP_005505.2:p.Ala329=