Canonical Allele Identifier: CA1619118254

Gene: HLA-B

Linked Data

• dbSNP Id: rs1766804766

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355155_31355156insAGC , CM000668.2:g.31355155_31355156insAGC	GRCh38
NC_000006.11:g.31322932_31322933insAGC , CM000668.1:g.31322932_31322933insAGC	GRCh37
NC_000006.10:g.31430911_31430912insAGC	NCBI36
NG_023187.1:g.7058_7059insCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3011_3012insCTG
ENST00000481849.6:n.2530_2531insCTG
ENST00000497377.6:n.2437_2438insCTG
ENST00000640094.2:c.895+162_895+163insCTG	ENSP00000491275.2:n.895+162_895+163insCTG
ENST00000696558.1:c.1033_1034insCTG	ENSP00000512716.1:n.1033_1034insCTG
ENST00000696559.1:c.964_965insCTG	ENSP00000512717.1:p.Val321_Val322insAla
ENST00000696560.1:c.964_965insCTG	ENSP00000512718.1:p.Val321_Val322insAla
ENST00000696561.1:c.964_965insCTG	ENSP00000512719.1:p.Val321_Val322insAla
ENST00000696562.1:c.964_965insCTG	ENSP00000512720.1:p.Val321_Val322insAla
ENST00000412585.7:c.964_965insCTG MANE Select	ENSP00000399168.2:p.Val321_Val322insAla
ENST00000640094.1:c.88+162_88+163insCTG	ENSP00000491275.1:n.88+162_88+163insCTG
ENST00000412585.6:c.964_965insCTG	ENSP00000399168.2:p.Val321_Val322insAla
ENST00000463574.1:n.555_556insCTG
NM_005514.6:c.964_965insCTG	NP_005505.2:p.Val321_Val322insAla
XM_011514556.1:c.997_998insCTG	XP_011512858.1:p.Val332_Val333insAla
XM_011514557.1:c.895+162_895+163insCTG	XP_011512859.1:n.895+162_895+163insCTG
XR_926175.1:n.1403_1404insCTG
NM_005514.7:c.964_965insCTG	NP_005505.2:p.Val321_Val322insAla
NM_005514.8:c.964_965insCTG MANE Select	NP_005505.2:p.Val321_Val322insAla