Canonical Allele Identifier: CA1087464888

Gene: HLA-B MIR6891

Linked Data

• gnomAD v3: 6-31355239-A-T
• gnomAD v4: 6-31355239-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355239A>T , CM000668.2:g.31355239A>T	GRCh38
NC_000006.11:g.31323016A>T , CM000668.1:g.31323016A>T	GRCh37
NC_000006.10:g.31430995A>T	NCBI36
NG_023187.1:g.6974T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2943-16T>A (HLA-B)
ENST00000481849.6:n.2446T>A (HLA-B)
ENST00000497377.6:n.2369-16T>A (HLA-B)
ENST00000640094.2:c.895+78T>A (HLA-B)	ENSP00000491275.2:n.895+78T>A
ENST00000696558.1:c.965-16T>A (HLA-B)	ENSP00000512716.1:n.965-16T>A
ENST00000696559.1:c.896-16T>A (HLA-B)	ENSP00000512717.1:n.896-16T>A
ENST00000696560.1:c.896-16T>A (HLA-B)	ENSP00000512718.1:n.896-16T>A
ENST00000696561.1:c.896-16T>A (HLA-B)	ENSP00000512719.1:n.896-16T>A
ENST00000696562.1:c.896-16T>A (HLA-B)	ENSP00000512720.1:n.896-16T>A
ENST00000412585.7:c.896-16T>A (HLA-B) MANE Select	ENSP00000399168.2:n.896-16T>A
ENST00000640094.1:c.88+78T>A (HLA-B)	ENSP00000491275.1:n.88+78T>A
ENST00000412585.6:c.896-16T>A (HLA-B)	ENSP00000399168.2:n.896-16T>A
ENST00000463574.1:n.487-16T>A (HLA-B)
NM_005514.6:c.896-16T>A (HLA-B)	NP_005505.2:n.896-16T>A
NR_106951.1:n.78T>A (MIR6891)
XM_011514556.1:c.929-16T>A (HLA-B)	XP_011512858.1:n.929-16T>A
XM_011514557.1:c.895+78T>A (HLA-B)	XP_011512859.1:n.895+78T>A
XR_926175.1:n.1335-16T>A (HLA-B)
NM_005514.7:c.896-16T>A (HLA-B)	NP_005505.2:n.896-16T>A
NM_005514.8:c.896-16T>A (HLA-B) MANE Select	NP_005505.2:n.896-16T>A