Canonical Allele Identifier: CA2677955622

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355817-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355817_31355818insC , CM000668.2:g.31355817_31355818insC	GRCh38
NC_000006.11:g.31323594_31323595insC , CM000668.1:g.31323594_31323595insC	GRCh37
NC_000006.10:g.31431573_31431574insC	NCBI36
NG_023187.1:g.6395_6396insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2441_2442insG
ENST00000481849.6:n.2093-226_2093-225insG
ENST00000497377.6:n.2093-226_2093-225insG
ENST00000640094.2:c.620-226_620-225insG	ENSP00000491275.2:n.620-226_620-225insG
ENST00000696558.1:c.620-12_620-11insG	ENSP00000512716.1:n.620-12_620-11insG
ENST00000696559.1:c.620-226_620-225insG	ENSP00000512717.1:n.620-226_620-225insG
ENST00000696560.1:c.620-226_620-225insG	ENSP00000512718.1:n.620-226_620-225insG
ENST00000696561.1:c.620-226_620-225insG	ENSP00000512719.1:n.620-226_620-225insG
ENST00000696562.1:c.620-226_620-225insG	ENSP00000512720.1:n.620-226_620-225insG
ENST00000412585.7:c.620-226_620-225insG MANE Select	ENSP00000399168.2:n.620-226_620-225insG
ENST00000412585.6:c.620-226_620-225insG	ENSP00000399168.2:n.620-226_620-225insG
ENST00000434333.1:c.653-226_653-225insG	ENSP00000405931.1:n.653-226_653-225insG
ENST00000474381.1:n.843_844insG
ENST00000498007.1:n.886-226_886-225insG
NM_005514.6:c.620-226_620-225insG	NP_005505.2:n.620-226_620-225insG
XM_011514556.1:c.653-226_653-225insG	XP_011512858.1:n.653-226_653-225insG
XM_011514557.1:c.620-226_620-225insG	XP_011512859.1:n.620-226_620-225insG
XR_926175.1:n.978_979insG
NM_005514.7:c.620-226_620-225insG	NP_005505.2:n.620-226_620-225insG
NM_005514.8:c.620-226_620-225insG MANE Select	NP_005505.2:n.620-226_620-225insG