Canonical Allele Identifier: CA2677956164

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356010-GAGGGGGCCCTCAGAGGAAACTCAGGAAAACTCATGCCATTCTCCATTCAAC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356011_31356061del , CM000668.2:g.31356011_31356061del	GRCh38
NC_000006.11:g.31323788_31323838del , CM000668.1:g.31323788_31323838del	GRCh37
NC_000006.10:g.31431767_31431817del	NCBI36
NG_023187.1:g.6152_6202del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2198_2248del
ENST00000481849.6:n.2092+106_2092+156del
ENST00000497377.6:n.2092+106_2092+156del
ENST00000640094.2:c.619+106_619+156del	ENSP00000491275.2:n.619+106_619+156del
ENST00000696558.1:c.619+106_619+156del	ENSP00000512716.1:n.619+106_619+156del
ENST00000696559.1:c.619+106_619+156del	ENSP00000512717.1:n.619+106_619+156del
ENST00000696560.1:c.619+106_619+156del	ENSP00000512718.1:n.619+106_619+156del
ENST00000696561.1:c.619+106_619+156del	ENSP00000512719.1:n.619+106_619+156del
ENST00000696562.1:c.619+106_619+156del	ENSP00000512720.1:n.619+106_619+156del
ENST00000412585.7:c.619+106_619+156del MANE Select	ENSP00000399168.2:n.619+106_619+156del
ENST00000412585.6:c.619+106_619+156del	ENSP00000399168.2:n.619+106_619+156del
ENST00000434333.1:c.652+106_652+156del	ENSP00000405931.1:n.652+106_652+156del
ENST00000474381.1:n.600_650del
ENST00000498007.1:n.885+106_885+156del
NM_005514.6:c.619+106_619+156del	NP_005505.2:n.619+106_619+156del
XM_011514556.1:c.652+106_652+156del	XP_011512858.1:n.652+106_652+156del
XM_011514557.1:c.619+106_619+156del	XP_011512859.1:n.619+106_619+156del
XR_926175.1:n.735_785del
NM_005514.7:c.619+106_619+156del	NP_005505.2:n.619+106_619+156del
NM_005514.8:c.619+106_619+156del MANE Select	NP_005505.2:n.619+106_619+156del