Canonical Allele Identifier: CA1087464729

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31355182-CAA-C
• gnomAD v4: 6-31355182-CAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355183_31355184del , CM000668.2:g.31355183_31355184del	GRCh38
NC_000006.11:g.31322960_31322961del , CM000668.1:g.31322960_31322961del	GRCh37
NC_000006.10:g.31430939_31430940del	NCBI36
NG_023187.1:g.7029_7030del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2982_2983del
ENST00000481849.6:n.2501_2502del
ENST00000497377.6:n.2408_2409del
ENST00000640094.2:c.895+133_895+134del	ENSP00000491275.2:n.895+133_895+134del
ENST00000696558.1:c.1004_1005del	ENSP00000512716.1:n.1004_1005del
ENST00000696559.1:c.935_936del	ENSP00000512717.1:p.Val312GlyfsTer21
ENST00000696560.1:c.935_936del	ENSP00000512718.1:p.Val312GlyfsTer21
ENST00000696561.1:c.935_936del	ENSP00000512719.1:p.Val312GlyfsTer21
ENST00000696562.1:c.935_936del	ENSP00000512720.1:p.Val312GlyfsTer21
ENST00000412585.7:c.935_936del MANE Select	ENSP00000399168.2:p.Val312GlyfsTer21
ENST00000640094.1:c.88+133_88+134del	ENSP00000491275.1:n.88+133_88+134del
ENST00000412585.6:c.935_936del	ENSP00000399168.2:p.Val312GlyfsTer21
ENST00000463574.1:n.526_527del
NM_005514.6:c.935_936del	NP_005505.2:p.Val312GlyfsTer21
XM_011514556.1:c.968_969del	XP_011512858.1:p.Val323GlyfsTer21
XM_011514557.1:c.895+133_895+134del	XP_011512859.1:n.895+133_895+134del
XR_926175.1:n.1374_1375del
NM_005514.7:c.935_936del	NP_005505.2:p.Val312GlyfsTer21
NM_005514.8:c.935_936del MANE Select	NP_005505.2:p.Val312GlyfsTer21