Canonical Allele Identifier: CA2677958297

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31357544-CCCCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357545_31357548del , CM000668.2:g.31357545_31357548del	GRCh38
NC_000006.11:g.31325322_31325325del , CM000668.1:g.31325322_31325325del	GRCh37
NC_000006.10:g.31433301_31433304del	NCBI36
NG_023187.1:g.4665_4668del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1338+66_1338+69del
ENST00000481849.6:n.1338+66_1338+69del
ENST00000497377.6:n.1338+66_1338+69del
ENST00000696559.1:c.-136+66_-136+69del	ENSP00000512717.1:n.-136+66_-136+69del
ENST00000696560.1:c.-136+66_-136+69del	ENSP00000512718.1:n.-136+66_-136+69del
ENST00000696561.1:c.-136+66_-136+69del	ENSP00000512719.1:n.-136+66_-136+69del
ENST00000696562.1:c.-135-255_-135-252del	ENSP00000512720.1:n.-135-255_-135-252del
ENST00000603274.1:n.899_902del
XR_926692.1:n.164+66_164+69del