Canonical Allele Identifier: CA136831188

Gene: HLA-B

Linked Data

• dbSNP Id: rs139093151
• gnomAD v2: 6-31321837-GC-G
• gnomAD v3: 6-31354060-GC-G
• gnomAD v4: 6-31354060-GC-G
• COSMIC: COSN18779926
• MyVariant Identifiers: chr6:g.31321838del (hg19) ; chr6:g.31354061del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354064del , CM000668.2:g.31354064del	GRCh38
NC_000006.11:g.31321841del , CM000668.1:g.31321841del	GRCh37
NC_000006.10:g.31429820del	NCBI36
NG_023187.1:g.8152del

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3376del
ENST00000481849.6:n.3336del
ENST00000497377.6:n.3243del
ENST00000696558.1:c.1398del	ENSP00000512716.1:n.1398del
ENST00000696559.1:c.*240del	ENSP00000512717.1:n.*240del
ENST00000696560.1:c.*240del	ENSP00000512718.1:n.*240del
ENST00000696561.1:c.*240del	ENSP00000512719.1:n.*240del
ENST00000696562.1:c.*240del	ENSP00000512720.1:n.*240del
ENST00000412585.7:c.*240del MANE Select	ENSP00000399168.2:n.*240del
ENST00000412585.6:c.*240del	ENSP00000399168.2:n.*240del
ENST00000481849.5:n.564del
ENST00000497377.5:n.728del
NM_005514.6:c.*240del	NP_005505.2:n.*240del
XM_011514556.1:c.*240del	XP_011512858.1:n.*240del
XM_011514557.1:c.*240del	XP_011512859.1:n.*240del
XR_926175.1:n.1768del
NM_005514.7:c.*240del	NP_005505.2:n.*240del
NM_005514.8:c.*240del MANE Select	NP_005505.2:n.*240del