Canonical Allele Identifier: CA566689366

Gene: HLA-B MIR6891

Linked Data

• dbSNP Id: rs1285281460
• gnomAD v2: 6-31323043-G-A
• gnomAD v3: 6-31355266-G-A
• gnomAD v4: 6-31355266-G-A
• MyVariant Identifiers: chr6:g.31323043G>A (hg19) ; chr6:g.31355266G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355266G>A , CM000668.2:g.31355266G>A	GRCh38
NC_000006.11:g.31323043G>A , CM000668.1:g.31323043G>A	GRCh37
NC_000006.10:g.31431022G>A	NCBI36
NG_023187.1:g.6947C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2943-43C>T (HLA-B)
ENST00000481849.6:n.2419C>T (HLA-B)
ENST00000497377.6:n.2369-43C>T (HLA-B)
ENST00000640094.2:c.895+51C>T (HLA-B)	ENSP00000491275.2:n.895+51C>T
ENST00000696558.1:c.965-43C>T (HLA-B)	ENSP00000512716.1:n.965-43C>T
ENST00000696559.1:c.896-43C>T (HLA-B)	ENSP00000512717.1:n.896-43C>T
ENST00000696560.1:c.896-43C>T (HLA-B)	ENSP00000512718.1:n.896-43C>T
ENST00000696561.1:c.896-43C>T (HLA-B)	ENSP00000512719.1:n.896-43C>T
ENST00000696562.1:c.896-43C>T (HLA-B)	ENSP00000512720.1:n.896-43C>T
ENST00000412585.7:c.896-43C>T (HLA-B) MANE Select	ENSP00000399168.2:n.896-43C>T
ENST00000640094.1:c.88+51C>T (HLA-B)	ENSP00000491275.1:n.88+51C>T
ENST00000412585.6:c.896-43C>T (HLA-B)	ENSP00000399168.2:n.896-43C>T
ENST00000463574.1:n.487-43C>T (HLA-B)
NM_005514.6:c.896-43C>T (HLA-B)	NP_005505.2:n.896-43C>T
NR_106951.1:n.51C>T (MIR6891)
XM_011514556.1:c.929-43C>T (HLA-B)	XP_011512858.1:n.929-43C>T
XM_011514557.1:c.895+51C>T (HLA-B)	XP_011512859.1:n.895+51C>T
XR_926175.1:n.1335-43C>T (HLA-B)
NM_005514.7:c.896-43C>T (HLA-B)	NP_005505.2:n.896-43C>T
NM_005514.8:c.896-43C>T (HLA-B) MANE Select	NP_005505.2:n.896-43C>T