Canonical Allele Identifier: CA566689363

Gene: HLA-B MIR6891

Linked Data

• dbSNP Id: rs1407539675
• gnomAD v2: 6-31323034-C-A
• gnomAD v3: 6-31355257-C-A
• gnomAD v4: 6-31355257-C-A
• MyVariant Identifiers: chr6:g.31323034C>A (hg19) ; chr6:g.31355257C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355257C>A , CM000668.2:g.31355257C>A	GRCh38
NC_000006.11:g.31323034C>A , CM000668.1:g.31323034C>A	GRCh37
NC_000006.10:g.31431013C>A	NCBI36
NG_023187.1:g.6956G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2943-34G>T (HLA-B)
ENST00000481849.6:n.2428G>T (HLA-B)
ENST00000497377.6:n.2369-34G>T (HLA-B)
ENST00000640094.2:c.895+60G>T (HLA-B)	ENSP00000491275.2:n.895+60G>T
ENST00000696558.1:c.965-34G>T (HLA-B)	ENSP00000512716.1:n.965-34G>T
ENST00000696559.1:c.896-34G>T (HLA-B)	ENSP00000512717.1:n.896-34G>T
ENST00000696560.1:c.896-34G>T (HLA-B)	ENSP00000512718.1:n.896-34G>T
ENST00000696561.1:c.896-34G>T (HLA-B)	ENSP00000512719.1:n.896-34G>T
ENST00000696562.1:c.896-34G>T (HLA-B)	ENSP00000512720.1:n.896-34G>T
ENST00000412585.7:c.896-34G>T (HLA-B) MANE Select	ENSP00000399168.2:n.896-34G>T
ENST00000640094.1:c.88+60G>T (HLA-B)	ENSP00000491275.1:n.88+60G>T
ENST00000412585.6:c.896-34G>T (HLA-B)	ENSP00000399168.2:n.896-34G>T
ENST00000463574.1:n.487-34G>T (HLA-B)
NM_005514.6:c.896-34G>T (HLA-B)	NP_005505.2:n.896-34G>T
NR_106951.1:n.60G>T (MIR6891)
XM_011514556.1:c.929-34G>T (HLA-B)	XP_011512858.1:n.929-34G>T
XM_011514557.1:c.895+60G>T (HLA-B)	XP_011512859.1:n.895+60G>T
XR_926175.1:n.1335-34G>T (HLA-B)
NM_005514.7:c.896-34G>T (HLA-B)	NP_005505.2:n.896-34G>T
NM_005514.8:c.896-34G>T (HLA-B) MANE Select	NP_005505.2:n.896-34G>T