Canonical Allele Identifier: CA2517514562

Gene: HLA-B MIR6891

Linked Data

• gnomAD v4: 6-31355287-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355287A>T , CM000668.2:g.31355287A>T	GRCh38
NC_000006.11:g.31323064A>T , CM000668.1:g.31323064A>T	GRCh37
NC_000006.10:g.31431043A>T	NCBI36
NG_023187.1:g.6926T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2942+30T>A (HLA-B)
ENST00000481849.6:n.2398T>A (HLA-B)
ENST00000497377.6:n.2368+30T>A (HLA-B)
ENST00000640094.2:c.895+30T>A (HLA-B)	ENSP00000491275.2:n.895+30T>A
ENST00000696558.1:c.964+30T>A (HLA-B)	ENSP00000512716.1:n.964+30T>A
ENST00000696559.1:c.895+30T>A (HLA-B)	ENSP00000512717.1:n.895+30T>A
ENST00000696560.1:c.895+30T>A (HLA-B)	ENSP00000512718.1:n.895+30T>A
ENST00000696561.1:c.895+30T>A (HLA-B)	ENSP00000512719.1:n.895+30T>A
ENST00000696562.1:c.895+30T>A (HLA-B)	ENSP00000512720.1:n.895+30T>A
ENST00000412585.7:c.895+30T>A (HLA-B) MANE Select	ENSP00000399168.2:n.895+30T>A
ENST00000640094.1:c.88+30T>A (HLA-B)	ENSP00000491275.1:n.88+30T>A
ENST00000412585.6:c.895+30T>A (HLA-B)	ENSP00000399168.2:n.895+30T>A
ENST00000463574.1:n.486+30T>A (HLA-B)
NM_005514.6:c.895+30T>A (HLA-B)	NP_005505.2:n.895+30T>A
NR_106951.1:n.30T>A (MIR6891)
XM_011514556.1:c.928+30T>A (HLA-B)	XP_011512858.1:n.928+30T>A
XM_011514557.1:c.895+30T>A (HLA-B)	XP_011512859.1:n.895+30T>A
XR_926175.1:n.1334+30T>A (HLA-B)
NM_005514.7:c.895+30T>A (HLA-B)	NP_005505.2:n.895+30T>A
NM_005514.8:c.895+30T>A (HLA-B) MANE Select	NP_005505.2:n.895+30T>A