Canonical Allele Identifier: CA2677957902

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31357113-CCG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357115_31357116del , CM000668.2:g.31357115_31357116del	GRCh38
NC_000006.11:g.31324892_31324893del , CM000668.1:g.31324892_31324893del	GRCh37
NC_000006.10:g.31432871_31432872del	NCBI36
NG_023187.1:g.5098_5099del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1517_1518del
ENST00000481849.6:n.1517_1518del
ENST00000497377.6:n.1517_1518del
ENST00000640094.2:c.44_45del	ENSP00000491275.2:p.Ala15GlyfsTer?
ENST00000696558.1:c.44_45del	ENSP00000512716.1:p.Ala15GlyfsTer?
ENST00000696559.1:c.44_45del	ENSP00000512717.1:p.Ala15GlyfsTer?
ENST00000696560.1:c.44_45del	ENSP00000512718.1:p.Ala15GlyfsTer?
ENST00000696561.1:c.44_45del	ENSP00000512719.1:p.Ala15GlyfsTer?
ENST00000696562.1:c.44_45del	ENSP00000512720.1:p.Ala15GlyfsTer?
ENST00000412585.7:c.44_45del MANE Select	ENSP00000399168.2:p.Ala15GlyfsTer?
ENST00000412585.6:c.44_45del	ENSP00000399168.2:p.Ala15GlyfsTer?
ENST00000434333.1:c.-52_-51del	ENSP00000405931.1:n.-52_-51del
ENST00000498007.1:n.65_66del
ENST00000603274.1:n.469_470del
NM_005514.6:c.44_45del	NP_005505.2:p.Ala15GlyfsTer?
XM_011514557.1:c.44_45del	XP_011512859.1:p.Ala15GlyfsTer?
XR_926175.1:n.54_55del
NM_005514.7:c.44_45del	NP_005505.2:p.Ala15GlyfsTer?
NM_005514.8:c.44_45del MANE Select	NP_005505.2:p.Ala15GlyfsTer?