Canonical Allele Identifier: CA1619118603

Gene: HLA-B MIR6891

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355304T= , CM000668.2:g.31355304T=	GRCh38
NC_000006.11:g.31323081T= , CM000668.1:g.31323081T=	GRCh37
NC_000006.10:g.31431060T=	NCBI36
NG_023187.1:g.6909A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2942+13A= (HLA-B)
ENST00000481849.6:n.2381A= (HLA-B)
ENST00000497377.6:n.2368+13A= (HLA-B)
ENST00000640094.2:c.895+13A= (HLA-B)	ENSP00000491275.2:n.895+13A=
ENST00000696558.1:c.964+13A= (HLA-B)	ENSP00000512716.1:n.964+13A=
ENST00000696559.1:c.895+13A= (HLA-B)	ENSP00000512717.1:n.895+13A=
ENST00000696560.1:c.895+13A= (HLA-B)	ENSP00000512718.1:n.895+13A=
ENST00000696561.1:c.895+13A= (HLA-B)	ENSP00000512719.1:n.895+13A=
ENST00000696562.1:c.895+13A= (HLA-B)	ENSP00000512720.1:n.895+13A=
ENST00000412585.7:c.895+13A= (HLA-B) MANE Select	ENSP00000399168.2:n.895+13A=
ENST00000640094.1:c.88+13A= (HLA-B)	ENSP00000491275.1:n.88+13A=
ENST00000412585.6:c.895+13A= (HLA-B)	ENSP00000399168.2:n.895+13A=
ENST00000463574.1:n.486+13A= (HLA-B)
NM_005514.6:c.895+13A= (HLA-B)	NP_005505.2:n.895+13A=
NR_106951.1:n.13A= (MIR6891)
XM_011514556.1:c.928+13A= (HLA-B)	XP_011512858.1:n.928+13A=
XM_011514557.1:c.895+13A= (HLA-B)	XP_011512859.1:n.895+13A=
XR_926175.1:n.1334+13A= (HLA-B)
NM_005514.7:c.895+13A= (HLA-B)	NP_005505.2:n.895+13A=
NM_005514.8:c.895+13A= (HLA-B) MANE Select	NP_005505.2:n.895+13A=