Canonical Allele Identifier: CA2677953247

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354230-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354231del , CM000668.2:g.31354231del	GRCh38
NC_000006.11:g.31322008del , CM000668.1:g.31322008del	GRCh37
NC_000006.10:g.31429987del	NCBI36
NG_023187.1:g.7982del

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3206del
ENST00000481849.6:n.3166del
ENST00000497377.6:n.3073del
ENST00000696558.1:c.1228del	ENSP00000512716.1:n.1228del
ENST00000696559.1:c.*70del	ENSP00000512717.1:n.*70del
ENST00000696560.1:c.*70del	ENSP00000512718.1:n.*70del
ENST00000696561.1:c.*70del	ENSP00000512719.1:n.*70del
ENST00000696562.1:c.*70del	ENSP00000512720.1:n.*70del
ENST00000412585.7:c.*70del MANE Select	ENSP00000399168.2:n.*70del
ENST00000412585.6:c.*70del	ENSP00000399168.2:n.*70del
ENST00000481849.5:n.394del
ENST00000497377.5:n.558del
NM_005514.6:c.*70del	NP_005505.2:n.*70del
XM_011514556.1:c.*70del	XP_011512858.1:n.*70del
XM_011514557.1:c.*70del	XP_011512859.1:n.*70del
XR_926175.1:n.1598del
NM_005514.7:c.*70del	NP_005505.2:n.*70del
NM_005514.8:c.*70del MANE Select	NP_005505.2:n.*70del