Canonical Allele Identifier: CA2677955065

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355164-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355165del , CM000668.2:g.31355165del	GRCh38
NC_000006.11:g.31322942del , CM000668.1:g.31322942del	GRCh37
NC_000006.10:g.31430921del	NCBI36
NG_023187.1:g.7048del

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3001del
ENST00000481849.6:n.2520del
ENST00000497377.6:n.2427del
ENST00000640094.2:c.895+152del	ENSP00000491275.2:n.895+152del
ENST00000696558.1:c.1023del	ENSP00000512716.1:n.1023del
ENST00000696559.1:c.954del	ENSP00000512717.1:p.Ala319GlnfsTer12
ENST00000696560.1:c.954del	ENSP00000512718.1:p.Ala319GlnfsTer12
ENST00000696561.1:c.954del	ENSP00000512719.1:p.Ala319GlnfsTer12
ENST00000696562.1:c.954del	ENSP00000512720.1:p.Ala319GlnfsTer12
ENST00000412585.7:c.954del MANE Select	ENSP00000399168.2:p.Ala319GlnfsTer12
ENST00000640094.1:c.88+152del	ENSP00000491275.1:n.88+152del
ENST00000412585.6:c.954del	ENSP00000399168.2:p.Ala319GlnfsTer12
ENST00000463574.1:n.545del
NM_005514.6:c.954del	NP_005505.2:p.Ala319GlnfsTer12
XM_011514556.1:c.987del	XP_011512858.1:p.Ala330GlnfsTer12
XM_011514557.1:c.895+152del	XP_011512859.1:n.895+152del
XR_926175.1:n.1393del
NM_005514.7:c.954del	NP_005505.2:p.Ala319GlnfsTer12
NM_005514.8:c.954del MANE Select	NP_005505.2:p.Ala319GlnfsTer12