Canonical Allele Identifier: CA2677955221

Gene: HLA-B MIR6891

Linked Data

• dbSNP Id: rs2113736110
• gnomAD v4: 6-31355260-G-GCTGAAGGGCTC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355264_31355274dup , CM000668.2:g.31355264_31355274dup	GRCh38
NC_000006.11:g.31323041_31323051dup , CM000668.1:g.31323041_31323051dup	GRCh37
NC_000006.10:g.31431020_31431030dup	NCBI36
NG_023187.1:g.6942_6952dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2942+46_2943-38dup (HLA-B)
ENST00000481849.6:n.2414_2424dup (HLA-B)
ENST00000497377.6:n.2368+46_2369-38dup (HLA-B)
ENST00000640094.2:c.895+46_895+56dup (HLA-B)	ENSP00000491275.2:n.895+46_895+56dup
ENST00000696558.1:c.964+46_965-38dup (HLA-B)	ENSP00000512716.1:n.964+46_965-38dup
ENST00000696559.1:c.895+46_896-38dup (HLA-B)	ENSP00000512717.1:n.895+46_896-38dup
ENST00000696560.1:c.895+46_896-38dup (HLA-B)	ENSP00000512718.1:n.895+46_896-38dup
ENST00000696561.1:c.895+46_896-38dup (HLA-B)	ENSP00000512719.1:n.895+46_896-38dup
ENST00000696562.1:c.895+46_896-38dup (HLA-B)	ENSP00000512720.1:n.895+46_896-38dup
ENST00000412585.7:c.895+46_896-38dup (HLA-B) MANE Select	ENSP00000399168.2:n.895+46_896-38dup
ENST00000640094.1:c.88+46_88+56dup (HLA-B)	ENSP00000491275.1:n.88+46_88+56dup
ENST00000412585.6:c.895+46_896-38dup (HLA-B)	ENSP00000399168.2:n.895+46_896-38dup
ENST00000463574.1:n.486+46_487-38dup (HLA-B)
NM_005514.6:c.895+46_896-38dup (HLA-B)	NP_005505.2:n.895+46_896-38dup
NR_106951.1:n.46_56dup (MIR6891)
XM_011514556.1:c.928+46_929-38dup (HLA-B)	XP_011512858.1:n.928+46_929-38dup
XM_011514557.1:c.895+46_895+56dup (HLA-B)	XP_011512859.1:n.895+46_895+56dup
XR_926175.1:n.1334+46_1335-38dup (HLA-B)
NM_005514.7:c.895+46_896-38dup (HLA-B)	NP_005505.2:n.895+46_896-38dup
NM_005514.8:c.895+46_896-38dup (HLA-B) MANE Select	NP_005505.2:n.895+46_896-38dup