Canonical Allele Identifier: CA2677957924

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31357151-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357153del , CM000668.2:g.31357153del	GRCh38
NC_000006.11:g.31324930del , CM000668.1:g.31324930del	GRCh37
NC_000006.10:g.31432909del	NCBI36
NG_023187.1:g.5061del

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1480del
ENST00000481849.6:n.1480del
ENST00000497377.6:n.1480del
ENST00000640094.2:c.7del	ENSP00000491275.2:p.Val3SerfsTer17
ENST00000696558.1:c.7del	ENSP00000512716.1:p.Val3SerfsTer17
ENST00000696559.1:c.7del	ENSP00000512717.1:p.Val3SerfsTer17
ENST00000696560.1:c.7del	ENSP00000512718.1:p.Val3SerfsTer17
ENST00000696561.1:c.7del	ENSP00000512719.1:p.Val3SerfsTer17
ENST00000696562.1:c.7del	ENSP00000512720.1:p.Val3SerfsTer17
ENST00000412585.7:c.7del MANE Select	ENSP00000399168.2:p.Val3SerfsTer17
ENST00000412585.6:c.7del	ENSP00000399168.2:p.Val3SerfsTer17
ENST00000434333.1:c.-89del	ENSP00000405931.1:n.-89del
ENST00000498007.1:n.28del
ENST00000603274.1:n.507del
NM_005514.6:c.7del	NP_005505.2:p.Val3SerfsTer17
XM_011514557.1:c.7del	XP_011512859.1:p.Val3SerfsTer17
XR_926175.1:n.17del
NM_005514.7:c.7del	NP_005505.2:p.Val3SerfsTer17
NM_005514.8:c.7del MANE Select	NP_005505.2:p.Val3SerfsTer17