Canonical Allele Identifier: CA823876875

Gene: HLA-B

Linked Data

• dbSNP Id: rs1282078601
• gnomAD v4: 6-31354120-AG-A
• MyVariant Identifiers: chr6:g.31321898del (hg19) ; chr6:g.31354121del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354124del , CM000668.2:g.31354124del	GRCh38
NC_000006.11:g.31321901del , CM000668.1:g.31321901del	GRCh37
NC_000006.10:g.31429880del	NCBI36
NG_023187.1:g.8092del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3316del
ENST00000481849.6:n.3276del
ENST00000497377.6:n.3183del
ENST00000696558.1:c.1338del	ENSP00000512716.1:n.1338del
ENST00000696559.1:c.*180del	ENSP00000512717.1:n.*180del
ENST00000696560.1:c.*180del	ENSP00000512718.1:n.*180del
ENST00000696561.1:c.*180del	ENSP00000512719.1:n.*180del
ENST00000696562.1:c.*180del	ENSP00000512720.1:n.*180del
ENST00000412585.7:c.*180del MANE Select	ENSP00000399168.2:n.*180del
ENST00000412585.6:c.*180del	ENSP00000399168.2:n.*180del
ENST00000481849.5:n.504del
ENST00000497377.5:n.668del
NM_005514.6:c.*180del	NP_005505.2:n.*180del
XM_011514556.1:c.*180del	XP_011512858.1:n.*180del
XM_011514557.1:c.*180del	XP_011512859.1:n.*180del
XR_926175.1:n.1708del
NM_005514.7:c.*180del	NP_005505.2:n.*180del
NM_005514.8:c.*180del MANE Select	NP_005505.2:n.*180del