Canonical Allele Identifier: CA1087465071

Gene: HLA-B MIR6891

Linked Data

• dbSNP Id: rs2113736338
• gnomAD v3: 6-31355270-T-TCCAGAAGGGCC
• gnomAD v4: 6-31355270-T-TCCAGAAGGGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355272_31355273insAGAAGGGCCCC , CM000668.2:g.31355272_31355273insAGAAGGGCCCC	GRCh38
NC_000006.11:g.31323049_31323050insAGAAGGGCCCC , CM000668.1:g.31323049_31323050insAGAAGGGCCCC	GRCh37
NC_000006.10:g.31431028_31431029insAGAAGGGCCCC	NCBI36
NG_023187.1:g.6942_6943insGGCCCTTCTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2942+46_2943-47insGGCCCTTCTGG (HLA-B)
ENST00000481849.6:n.2414_2415insGGCCCTTCTGG (HLA-B)
ENST00000497377.6:n.2368+46_2369-47insGGCCCTTCTGG (HLA-B)
ENST00000640094.2:c.895+46_895+47insGGCCCTTCTGG (HLA-B)	ENSP00000491275.2:n.895+46_895+47insGGCCCTTCTGG
ENST00000696558.1:c.964+46_965-47insGGCCCTTCTGG (HLA-B)	ENSP00000512716.1:n.964+46_965-47insGGCCCTTCTGG
ENST00000696559.1:c.895+46_896-47insGGCCCTTCTGG (HLA-B)	ENSP00000512717.1:n.895+46_896-47insGGCCCTTCTGG
ENST00000696560.1:c.895+46_896-47insGGCCCTTCTGG (HLA-B)	ENSP00000512718.1:n.895+46_896-47insGGCCCTTCTGG
ENST00000696561.1:c.895+46_896-47insGGCCCTTCTGG (HLA-B)	ENSP00000512719.1:n.895+46_896-47insGGCCCTTCTGG
ENST00000696562.1:c.895+46_896-47insGGCCCTTCTGG (HLA-B)	ENSP00000512720.1:n.895+46_896-47insGGCCCTTCTGG
ENST00000412585.7:c.895+46_896-47insGGCCCTTCTGG (HLA-B) MANE Select	ENSP00000399168.2:n.895+46_896-47insGGCCCTTCTGG
ENST00000640094.1:c.88+46_88+47insGGCCCTTCTGG (HLA-B)	ENSP00000491275.1:n.88+46_88+47insGGCCCTTCTGG
ENST00000412585.6:c.895+46_896-47insGGCCCTTCTGG (HLA-B)	ENSP00000399168.2:n.895+46_896-47insGGCCCTTCTGG
ENST00000463574.1:n.486+46_487-47insGGCCCTTCTGG (HLA-B)
NM_005514.6:c.895+46_896-47insGGCCCTTCTGG (HLA-B)	NP_005505.2:n.895+46_896-47insGGCCCTTCTGG
NR_106951.1:n.46_47insGGCCCTTCTGG (MIR6891)
XM_011514556.1:c.928+46_929-47insGGCCCTTCTGG (HLA-B)	XP_011512858.1:n.928+46_929-47insGGCCCTTCTGG
XM_011514557.1:c.895+46_895+47insGGCCCTTCTGG (HLA-B)	XP_011512859.1:n.895+46_895+47insGGCCCTTCTGG
XR_926175.1:n.1334+46_1335-47insGGCCCTTCTGG (HLA-B)
NM_005514.7:c.895+46_896-47insGGCCCTTCTGG (HLA-B)	NP_005505.2:n.895+46_896-47insGGCCCTTCTGG
NM_005514.8:c.895+46_896-47insGGCCCTTCTGG (HLA-B) MANE Select	NP_005505.2:n.895+46_896-47insGGCCCTTCTGG