Canonical Allele Identifier: CA2677957932

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31357175-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357176del , CM000668.2:g.31357176del	GRCh38
NC_000006.11:g.31324953del , CM000668.1:g.31324953del	GRCh37
NC_000006.10:g.31432932del	NCBI36
NG_023187.1:g.5037del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1456del
ENST00000481849.6:n.1456del
ENST00000497377.6:n.1456del
ENST00000696559.1:c.-18del	ENSP00000512717.1:n.-18del
ENST00000696560.1:c.-18del	ENSP00000512718.1:n.-18del
ENST00000696561.1:c.-18del	ENSP00000512719.1:n.-18del
ENST00000696562.1:c.-18del	ENSP00000512720.1:n.-18del
ENST00000412585.7:c.-18del MANE Select	ENSP00000399168.2:n.-18del
ENST00000412585.6:c.-18del	ENSP00000399168.2:n.-18del
ENST00000434333.1:c.-113del	ENSP00000405931.1:n.-113del
ENST00000498007.1:n.4del
ENST00000603274.1:n.530del
NM_005514.6:c.-18del	NP_005505.2:n.-18del
NM_005514.7:c.-18del	NP_005505.2:n.-18del
NM_005514.8:c.-18del MANE Select	NP_005505.2:n.-18del