Canonical Allele Identifier: CA566689355

Gene: HLA-B

Linked Data

• dbSNP Id: rs1294780926
• gnomAD v2: 6-31322864-AC-A
• gnomAD v4: 6-31355087-AC-A
• MyVariant Identifiers: chr6:g.31322865del (hg19) ; chr6:g.31355088del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355091del , CM000668.2:g.31355091del	GRCh38
NC_000006.11:g.31322868del , CM000668.1:g.31322868del	GRCh37
NC_000006.10:g.31430847del	NCBI36
NG_023187.1:g.7125del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3059+19del
ENST00000481849.6:n.2597del
ENST00000497377.6:n.2504del
ENST00000640094.2:c.895+229del	ENSP00000491275.2:n.895+229del
ENST00000696558.1:c.1081+19del	ENSP00000512716.1:n.1081+19del
ENST00000696559.1:c.1012+19del	ENSP00000512717.1:n.1012+19del
ENST00000696560.1:c.1012+19del	ENSP00000512718.1:n.1012+19del
ENST00000696561.1:c.1012+19del	ENSP00000512719.1:n.1012+19del
ENST00000696562.1:c.1012+19del	ENSP00000512720.1:n.1012+19del
ENST00000412585.7:c.1012+19del MANE Select	ENSP00000399168.2:n.1012+19del
ENST00000640094.1:c.88+229del	ENSP00000491275.1:n.88+229del
ENST00000412585.6:c.1012+19del	ENSP00000399168.2:n.1012+19del
NM_005514.6:c.1012+19del	NP_005505.2:n.1012+19del
XM_011514556.1:c.1045+19del	XP_011512858.1:n.1045+19del
XM_011514557.1:c.895+229del	XP_011512859.1:n.895+229del
XR_926175.1:n.1451+19del
NM_005514.7:c.1012+19del	NP_005505.2:n.1012+19del
NM_005514.8:c.1012+19del MANE Select	NP_005505.2:n.1012+19del