Canonical Allele Identifier: CA2677955071

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355167-G-GGT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355168_31355169insTG , CM000668.2:g.31355168_31355169insTG	GRCh38
NC_000006.11:g.31322945_31322946insTG , CM000668.1:g.31322945_31322946insTG	GRCh37
NC_000006.10:g.31430924_31430925insTG	NCBI36
NG_023187.1:g.7045_7046insAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2998_2999insAC
ENST00000481849.6:n.2517_2518insAC
ENST00000497377.6:n.2424_2425insAC
ENST00000640094.2:c.895+149_895+150insAC	ENSP00000491275.2:n.895+149_895+150insAC
ENST00000696558.1:c.1020_1021insAC	ENSP00000512716.1:n.1020_1021insAC
ENST00000696559.1:c.951_952insAC	ENSP00000512717.1:p.Leu318ThrfsTer2
ENST00000696560.1:c.951_952insAC	ENSP00000512718.1:p.Leu318ThrfsTer2
ENST00000696561.1:c.951_952insAC	ENSP00000512719.1:p.Leu318ThrfsTer2
ENST00000696562.1:c.951_952insAC	ENSP00000512720.1:p.Leu318ThrfsTer2
ENST00000412585.7:c.951_952insAC MANE Select	ENSP00000399168.2:p.Leu318ThrfsTer2
ENST00000640094.1:c.88+149_88+150insAC	ENSP00000491275.1:n.88+149_88+150insAC
ENST00000412585.6:c.951_952insAC	ENSP00000399168.2:p.Leu318ThrfsTer2
ENST00000463574.1:n.542_543insAC
NM_005514.6:c.951_952insAC	NP_005505.2:p.Leu318ThrfsTer2
XM_011514556.1:c.984_985insAC	XP_011512858.1:p.Leu329ThrfsTer2
XM_011514557.1:c.895+149_895+150insAC	XP_011512859.1:n.895+149_895+150insAC
XR_926175.1:n.1390_1391insAC
NM_005514.7:c.951_952insAC	NP_005505.2:p.Leu318ThrfsTer2
NM_005514.8:c.951_952insAC MANE Select	NP_005505.2:p.Leu318ThrfsTer2