Canonical Allele Identifier: CA2677955242

Gene: HLA-B MIR6891

Linked Data

• gnomAD v4: 6-31355262-T-TGAAGCGCTCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355266_31355267insCGCTCCAGAAG , CM000668.2:g.31355266_31355267insCGCTCCAGAAG	GRCh38
NC_000006.11:g.31323043_31323044insCGCTCCAGAAG , CM000668.1:g.31323043_31323044insCGCTCCAGAAG	GRCh37
NC_000006.10:g.31431022_31431023insCGCTCCAGAAG	NCBI36
NG_023187.1:g.6950_6951insTGGAGCGCTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2943-40_2943-39insTGGAGCGCTTC (HLA-B)
ENST00000481849.6:n.2422_2423insTGGAGCGCTTC (HLA-B)
ENST00000497377.6:n.2369-40_2369-39insTGGAGCGCTTC (HLA-B)
ENST00000640094.2:c.895+54_895+55insTGGAGCGCTTC (HLA-B)	ENSP00000491275.2:n.895+54_895+55insTGGAGCGCTTC
ENST00000696558.1:c.965-40_965-39insTGGAGCGCTTC (HLA-B)	ENSP00000512716.1:n.965-40_965-39insTGGAGCGCTTC
ENST00000696559.1:c.896-40_896-39insTGGAGCGCTTC (HLA-B)	ENSP00000512717.1:n.896-40_896-39insTGGAGCGCTTC
ENST00000696560.1:c.896-40_896-39insTGGAGCGCTTC (HLA-B)	ENSP00000512718.1:n.896-40_896-39insTGGAGCGCTTC
ENST00000696561.1:c.896-40_896-39insTGGAGCGCTTC (HLA-B)	ENSP00000512719.1:n.896-40_896-39insTGGAGCGCTTC
ENST00000696562.1:c.896-40_896-39insTGGAGCGCTTC (HLA-B)	ENSP00000512720.1:n.896-40_896-39insTGGAGCGCTTC
ENST00000412585.7:c.896-40_896-39insTGGAGCGCTTC (HLA-B) MANE Select	ENSP00000399168.2:n.896-40_896-39insTGGAGCGCTTC
ENST00000640094.1:c.88+54_88+55insTGGAGCGCTTC (HLA-B)	ENSP00000491275.1:n.88+54_88+55insTGGAGCGCTTC
ENST00000412585.6:c.896-40_896-39insTGGAGCGCTTC (HLA-B)	ENSP00000399168.2:n.896-40_896-39insTGGAGCGCTTC
ENST00000463574.1:n.487-40_487-39insTGGAGCGCTTC (HLA-B)
NM_005514.6:c.896-40_896-39insTGGAGCGCTTC (HLA-B)	NP_005505.2:n.896-40_896-39insTGGAGCGCTTC
NR_106951.1:n.54_55insTGGAGCGCTTC (MIR6891)
XM_011514556.1:c.929-40_929-39insTGGAGCGCTTC (HLA-B)	XP_011512858.1:n.929-40_929-39insTGGAGCGCTTC
XM_011514557.1:c.895+54_895+55insTGGAGCGCTTC (HLA-B)	XP_011512859.1:n.895+54_895+55insTGGAGCGCTTC
XR_926175.1:n.1335-40_1335-39insTGGAGCGCTTC (HLA-B)
NM_005514.7:c.896-40_896-39insTGGAGCGCTTC (HLA-B)	NP_005505.2:n.896-40_896-39insTGGAGCGCTTC
NM_005514.8:c.896-40_896-39insTGGAGCGCTTC (HLA-B) MANE Select	NP_005505.2:n.896-40_896-39insTGGAGCGCTTC