Canonical Allele Identifier: CA1619119982

Gene: HLA-B

Linked Data

• dbSNP Id: rs1766934202
• gnomAD v4: 6-31356097-CCTCTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356101_31356105del , CM000668.2:g.31356101_31356105del	GRCh38
NC_000006.11:g.31323878_31323882del , CM000668.1:g.31323878_31323882del	GRCh37
NC_000006.10:g.31431857_31431861del	NCBI36
NG_023187.1:g.6111_6115del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2157_2161del
ENST00000481849.6:n.2092+65_2092+69del
ENST00000497377.6:n.2092+65_2092+69del
ENST00000640094.2:c.619+65_619+69del	ENSP00000491275.2:n.619+65_619+69del
ENST00000696558.1:c.619+65_619+69del	ENSP00000512716.1:n.619+65_619+69del
ENST00000696559.1:c.619+65_619+69del	ENSP00000512717.1:n.619+65_619+69del
ENST00000696560.1:c.619+65_619+69del	ENSP00000512718.1:n.619+65_619+69del
ENST00000696561.1:c.619+65_619+69del	ENSP00000512719.1:n.619+65_619+69del
ENST00000696562.1:c.619+65_619+69del	ENSP00000512720.1:n.619+65_619+69del
ENST00000412585.7:c.619+65_619+69del MANE Select	ENSP00000399168.2:n.619+65_619+69del
ENST00000412585.6:c.619+65_619+69del	ENSP00000399168.2:n.619+65_619+69del
ENST00000434333.1:c.652+65_652+69del	ENSP00000405931.1:n.652+65_652+69del
ENST00000474381.1:n.559_563del
ENST00000498007.1:n.885+65_885+69del
NM_005514.6:c.619+65_619+69del	NP_005505.2:n.619+65_619+69del
XM_011514556.1:c.652+65_652+69del	XP_011512858.1:n.652+65_652+69del
XM_011514557.1:c.619+65_619+69del	XP_011512859.1:n.619+65_619+69del
XR_926175.1:n.694_698del
NM_005514.7:c.619+65_619+69del	NP_005505.2:n.619+65_619+69del
NM_005514.8:c.619+65_619+69del MANE Select	NP_005505.2:n.619+65_619+69del