Canonical Allele Identifier: CA1087465016

Gene: HLA-B MIR6891

Linked Data

• dbSNP Id: rs1766827125
• gnomAD v3: 6-31355264-A-AAGGGCTCCAGG
• gnomAD v4: 6-31355264-A-AAGGGCTCCAGG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355272_31355273insAGGAGGGCTCC , CM000668.2:g.31355272_31355273insAGGAGGGCTCC	GRCh38
NC_000006.11:g.31323049_31323050insAGGAGGGCTCC , CM000668.1:g.31323049_31323050insAGGAGGGCTCC	GRCh37
NC_000006.10:g.31431028_31431029insAGGAGGGCTCC	NCBI36
NG_023187.1:g.6948_6949insCCTGGAGCCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2943-42_2943-41insCCTGGAGCCCT (HLA-B)
ENST00000481849.6:n.2420_2421insCCTGGAGCCCT (HLA-B)
ENST00000497377.6:n.2369-42_2369-41insCCTGGAGCCCT (HLA-B)
ENST00000640094.2:c.895+52_895+53insCCTGGAGCCCT (HLA-B)	ENSP00000491275.2:n.895+52_895+53insCCTGGAGCCCT
ENST00000696558.1:c.965-42_965-41insCCTGGAGCCCT (HLA-B)	ENSP00000512716.1:n.965-42_965-41insCCTGGAGCCCT
ENST00000696559.1:c.896-42_896-41insCCTGGAGCCCT (HLA-B)	ENSP00000512717.1:n.896-42_896-41insCCTGGAGCCCT
ENST00000696560.1:c.896-42_896-41insCCTGGAGCCCT (HLA-B)	ENSP00000512718.1:n.896-42_896-41insCCTGGAGCCCT
ENST00000696561.1:c.896-42_896-41insCCTGGAGCCCT (HLA-B)	ENSP00000512719.1:n.896-42_896-41insCCTGGAGCCCT
ENST00000696562.1:c.896-42_896-41insCCTGGAGCCCT (HLA-B)	ENSP00000512720.1:n.896-42_896-41insCCTGGAGCCCT
ENST00000412585.7:c.896-42_896-41insCCTGGAGCCCT (HLA-B) MANE Select	ENSP00000399168.2:n.896-42_896-41insCCTGGAGCCCT
ENST00000640094.1:c.88+52_88+53insCCTGGAGCCCT (HLA-B)	ENSP00000491275.1:n.88+52_88+53insCCTGGAGCCCT
ENST00000412585.6:c.896-42_896-41insCCTGGAGCCCT (HLA-B)	ENSP00000399168.2:n.896-42_896-41insCCTGGAGCCCT
ENST00000463574.1:n.487-42_487-41insCCTGGAGCCCT (HLA-B)
NM_005514.6:c.896-42_896-41insCCTGGAGCCCT (HLA-B)	NP_005505.2:n.896-42_896-41insCCTGGAGCCCT
NR_106951.1:n.52_53insCCTGGAGCCCT (MIR6891)
XM_011514556.1:c.929-42_929-41insCCTGGAGCCCT (HLA-B)	XP_011512858.1:n.929-42_929-41insCCTGGAGCCCT
XM_011514557.1:c.895+52_895+53insCCTGGAGCCCT (HLA-B)	XP_011512859.1:n.895+52_895+53insCCTGGAGCCCT
XR_926175.1:n.1335-42_1335-41insCCTGGAGCCCT (HLA-B)
NM_005514.7:c.896-42_896-41insCCTGGAGCCCT (HLA-B)	NP_005505.2:n.896-42_896-41insCCTGGAGCCCT
NM_005514.8:c.896-42_896-41insCCTGGAGCCCT (HLA-B) MANE Select	NP_005505.2:n.896-42_896-41insCCTGGAGCCCT