Canonical Allele Identifier: CA1619118547

Gene: HLA-B MIR6891

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355274_31355275delinsGC , CM000668.2:g.31355274_31355275delinsGC	GRCh38
NC_000006.11:g.31323051_31323052delinsGC , CM000668.1:g.31323051_31323052delinsGC	GRCh37
NC_000006.10:g.31431030_31431031delinsGC	NCBI36
NG_023187.1:g.6938_6939delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2942+42_2942+43delinsGC (HLA-B)
ENST00000481849.6:n.2410_2411delinsGC (HLA-B)
ENST00000497377.6:n.2368+42_2368+43delinsGC (HLA-B)
ENST00000640094.2:c.895+42_895+43delinsGC (HLA-B)	ENSP00000491275.2:n.895+42_895+43delinsGC
ENST00000696558.1:c.964+42_964+43delinsGC (HLA-B)	ENSP00000512716.1:n.964+42_964+43delinsGC
ENST00000696559.1:c.895+42_895+43delinsGC (HLA-B)	ENSP00000512717.1:n.895+42_895+43delinsGC
ENST00000696560.1:c.895+42_895+43delinsGC (HLA-B)	ENSP00000512718.1:n.895+42_895+43delinsGC
ENST00000696561.1:c.895+42_895+43delinsGC (HLA-B)	ENSP00000512719.1:n.895+42_895+43delinsGC
ENST00000696562.1:c.895+42_895+43delinsGC (HLA-B)	ENSP00000512720.1:n.895+42_895+43delinsGC
ENST00000412585.7:c.895+42_895+43delinsGC (HLA-B) MANE Select	ENSP00000399168.2:n.895+42_895+43delinsGC
ENST00000640094.1:c.88+42_88+43delinsGC (HLA-B)	ENSP00000491275.1:n.88+42_88+43delinsGC
ENST00000412585.6:c.895+42_895+43delinsGC (HLA-B)	ENSP00000399168.2:n.895+42_895+43delinsGC
ENST00000463574.1:n.486+42_486+43delinsGC (HLA-B)
NM_005514.6:c.895+42_895+43delinsGC (HLA-B)	NP_005505.2:n.895+42_895+43delinsGC
NR_106951.1:n.42_43delinsGC (MIR6891)
XM_011514556.1:c.928+42_928+43delinsGC (HLA-B)	XP_011512858.1:n.928+42_928+43delinsGC
XM_011514557.1:c.895+42_895+43delinsGC (HLA-B)	XP_011512859.1:n.895+42_895+43delinsGC
XR_926175.1:n.1334+42_1334+43delinsGC (HLA-B)
NM_005514.7:c.895+42_895+43delinsGC (HLA-B)	NP_005505.2:n.895+42_895+43delinsGC
NM_005514.8:c.895+42_895+43delinsGC (HLA-B) MANE Select	NP_005505.2:n.895+42_895+43delinsGC