Canonical Allele Identifier: CA2677955117

Gene: HLA-B MIR6891

Linked Data

• gnomAD v4: 6-31355225-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355228dup , CM000668.2:g.31355228dup	GRCh38
NC_000006.11:g.31323005dup , CM000668.1:g.31323005dup	GRCh37
NC_000006.10:g.31430984dup	NCBI36
NG_023187.1:g.6987dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2943-3dup (HLA-B)
ENST00000481849.6:n.2459dup (HLA-B)
ENST00000497377.6:n.2369-3dup (HLA-B)
ENST00000640094.2:c.895+91dup (HLA-B)	ENSP00000491275.2:n.895+91dup
ENST00000696558.1:c.965-3dup (HLA-B)	ENSP00000512716.1:n.965-3dup
ENST00000696559.1:c.896-3dup (HLA-B)	ENSP00000512717.1:n.896-3dup
ENST00000696560.1:c.896-3dup (HLA-B)	ENSP00000512718.1:n.896-3dup
ENST00000696561.1:c.896-3dup (HLA-B)	ENSP00000512719.1:n.896-3dup
ENST00000696562.1:c.896-3dup (HLA-B)	ENSP00000512720.1:n.896-3dup
ENST00000412585.7:c.896-3dup (HLA-B) MANE Select	ENSP00000399168.2:n.896-3dup
ENST00000640094.1:c.88+91dup (HLA-B)	ENSP00000491275.1:n.88+91dup
ENST00000412585.6:c.896-3dup (HLA-B)	ENSP00000399168.2:n.896-3dup
ENST00000463574.1:n.487-3dup (HLA-B)
NM_005514.6:c.896-3dup (HLA-B)	NP_005505.2:n.896-3dup
NR_106951.1:n.91dup (MIR6891)
XM_011514556.1:c.929-3dup (HLA-B)	XP_011512858.1:n.929-3dup
XM_011514557.1:c.895+91dup (HLA-B)	XP_011512859.1:n.895+91dup
XR_926175.1:n.1335-3dup (HLA-B)
NM_005514.7:c.896-3dup (HLA-B)	NP_005505.2:n.896-3dup
NM_005514.8:c.896-3dup (HLA-B) MANE Select	NP_005505.2:n.896-3dup