Canonical Allele Identifier: CA1619114303

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357131_31357134delinsGGAC , CM000668.2:g.31357131_31357134delinsGGAC	GRCh38
NC_000006.11:g.31324908_31324911delinsGGAC , CM000668.1:g.31324908_31324911delinsGGAC	GRCh37
NC_000006.10:g.31432887_31432890delinsGGAC	NCBI36
NG_023187.1:g.5079_5082delinsGTCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1498_1501delinsGTCC
ENST00000481849.6:n.1498_1501delinsGTCC
ENST00000497377.6:n.1498_1501delinsGTCC
ENST00000640094.2:c.25_28delinsGTCC	ENSP00000491275.2:p.Val9=
ENST00000696558.1:c.25_28delinsGTCC	ENSP00000512716.1:p.Val9=
ENST00000696559.1:c.25_28delinsGTCC	ENSP00000512717.1:p.Val9=
ENST00000696560.1:c.25_28delinsGTCC	ENSP00000512718.1:p.Val9=
ENST00000696561.1:c.25_28delinsGTCC	ENSP00000512719.1:p.Val9=
ENST00000696562.1:c.25_28delinsGTCC	ENSP00000512720.1:p.Val9=
ENST00000412585.7:c.25_28delinsGTCC MANE Select	ENSP00000399168.2:p.Val9=
ENST00000412585.6:c.25_28delinsGTCC	ENSP00000399168.2:p.Val9=
ENST00000434333.1:c.-71_-68delinsGTCC	ENSP00000405931.1:n.-71_-68delinsGTCC
ENST00000498007.1:n.46_49delinsGTCC
ENST00000603274.1:n.485_488delinsGGAC
NM_005514.6:c.25_28delinsGTCC	NP_005505.2:p.Val9=
XM_011514557.1:c.25_28delinsGTCC	XP_011512859.1:p.Val9=
XR_926175.1:n.35_38delinsGTCC
NM_005514.7:c.25_28delinsGTCC	NP_005505.2:p.Val9=
NM_005514.8:c.25_28delinsGTCC MANE Select	NP_005505.2:p.Val9=