Canonical Allele Identifier: CA1619114922

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357541_31357543delinsCAG , CM000668.2:g.31357541_31357543delinsCAG	GRCh38
NC_000006.11:g.31325318_31325320delinsCAG , CM000668.1:g.31325318_31325320delinsCAG	GRCh37
NC_000006.10:g.31433297_31433299delinsCAG	NCBI36
NG_023187.1:g.4670_4672delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1338+71_1338+73delinsCTG
ENST00000481849.6:n.1338+71_1338+73delinsCTG
ENST00000497377.6:n.1338+71_1338+73delinsCTG
ENST00000696559.1:c.-136+71_-136+73delinsCTG	ENSP00000512717.1:n.-136+71_-136+73delinsCTG
ENST00000696560.1:c.-136+71_-136+73delinsCTG	ENSP00000512718.1:n.-136+71_-136+73delinsCTG
ENST00000696561.1:c.-136+71_-136+73delinsCTG	ENSP00000512719.1:n.-136+71_-136+73delinsCTG
ENST00000696562.1:c.-135-250_-135-248delinsCTG	ENSP00000512720.1:n.-135-250_-135-248delinsCTG
ENST00000603274.1:n.895_897delinsCAG
XR_926692.1:n.164+71_164+73delinsCTG