Canonical Allele Identifier: CA917712347

Gene: HLA-B

Linked Data

• dbSNP Id: rs1554212100
• gnomAD v3: 6-31356751-G-GGT
• gnomAD v4: 6-31356751-G-GGT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356752_31356753insTG , CM000668.2:g.31356752_31356753insTG	GRCh38
NC_000006.11:g.31324529_31324530insTG , CM000668.1:g.31324529_31324530insTG	GRCh37
NC_000006.10:g.31432508_31432509insTG	NCBI36
NG_023187.1:g.5461_5462insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1752_1753insAC
ENST00000481849.6:n.1752_1753insAC
ENST00000497377.6:n.1752_1753insAC
ENST00000640094.2:c.279_280insAC	ENSP00000491275.2:p.Gln94ThrfsTer?
ENST00000696558.1:c.279_280insAC	ENSP00000512716.1:p.Gln94ThrfsTer?
ENST00000696559.1:c.279_280insAC	ENSP00000512717.1:p.Gln94ThrfsTer?
ENST00000696560.1:c.279_280insAC	ENSP00000512718.1:p.Gln94ThrfsTer?
ENST00000696561.1:c.279_280insAC	ENSP00000512719.1:p.Gln94ThrfsTer?
ENST00000696562.1:c.279_280insAC	ENSP00000512720.1:p.Gln94ThrfsTer?
ENST00000412585.7:c.279_280insAC MANE Select	ENSP00000399168.2:p.Gln94ThrfsTer?
ENST00000412585.6:c.279_280insAC	ENSP00000399168.2:p.Gln94ThrfsTer?
ENST00000434333.1:c.312_313insAC	ENSP00000405931.1:p.Gln105ThrfsTer?
ENST00000474381.1:n.154_155insAC
ENST00000498007.1:n.300_301insAC
ENST00000603274.1:n.106_107insTG
NM_005514.6:c.279_280insAC	NP_005505.2:p.Gln94ThrfsTer?
XM_011514556.1:c.312_313insAC	XP_011512858.1:p.Gln105ThrfsTer?
XM_011514557.1:c.279_280insAC	XP_011512859.1:p.Gln94ThrfsTer?
XR_926175.1:n.289_290insAC
NM_005514.7:c.279_280insAC	NP_005505.2:p.Gln94ThrfsTer?
NM_005514.8:c.279_280insAC MANE Select	NP_005505.2:p.Gln94ThrfsTer?