Canonical Allele Identifier: CA2677956568

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356184-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356186del , CM000668.2:g.31356186del	GRCh38
NC_000006.11:g.31323963del , CM000668.1:g.31323963del	GRCh37
NC_000006.10:g.31431942del	NCBI36
NG_023187.1:g.6028del

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2074del
ENST00000481849.6:n.2074del
ENST00000497377.6:n.2074del
ENST00000640094.2:c.601del	ENSP00000491275.2:p.Asp201ThrfsTer13
ENST00000696558.1:c.601del	ENSP00000512716.1:p.Asp201ThrfsTer?
ENST00000696559.1:c.601del	ENSP00000512717.1:p.Asp201ThrfsTer13
ENST00000696560.1:c.601del	ENSP00000512718.1:p.Asp201ThrfsTer13
ENST00000696561.1:c.601del	ENSP00000512719.1:p.Asp201ThrfsTer13
ENST00000696562.1:c.601del	ENSP00000512720.1:p.Asp201ThrfsTer13
ENST00000412585.7:c.601del MANE Select	ENSP00000399168.2:p.Asp201ThrfsTer13
ENST00000412585.6:c.601del	ENSP00000399168.2:p.Asp201ThrfsTer13
ENST00000434333.1:c.634del	ENSP00000405931.1:p.Asp212ThrfsTer13
ENST00000474381.1:n.476del
ENST00000498007.1:n.867del
NM_005514.6:c.601del	NP_005505.2:p.Asp201ThrfsTer13
XM_011514556.1:c.634del	XP_011512858.1:p.Asp212ThrfsTer13
XM_011514557.1:c.601del	XP_011512859.1:p.Asp201ThrfsTer13
XR_926175.1:n.611del
NM_005514.7:c.601del	NP_005505.2:p.Asp201ThrfsTer13
NM_005514.8:c.601del MANE Select	NP_005505.2:p.Asp201ThrfsTer13