Canonical Allele Identifier: CA3711314

Gene: HLA-B MIR6891

Linked Data

• dbSNP Id: rs17881225
• ExAC: 6:31323065 G / C
• gnomAD v2: 6-31323065-G-C
• gnomAD v3: 6-31355288-G-C
• gnomAD v4: 6-31355288-G-C
• MyVariant Identifiers: chr6:g.31323065G>C (hg19) ; chr6:g.31355288G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355288G>C , CM000668.2:g.31355288G>C	GRCh38
NC_000006.11:g.31323065G>C , CM000668.1:g.31323065G>C	GRCh37
NC_000006.10:g.31431044G>C	NCBI36
NG_023187.1:g.6925C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2942+29C>G (HLA-B)
ENST00000481849.6:n.2397C>G (HLA-B)
ENST00000497377.6:n.2368+29C>G (HLA-B)
ENST00000640094.2:c.895+29C>G (HLA-B)	ENSP00000491275.2:n.895+29C>G
ENST00000696558.1:c.964+29C>G (HLA-B)	ENSP00000512716.1:n.964+29C>G
ENST00000696559.1:c.895+29C>G (HLA-B)	ENSP00000512717.1:n.895+29C>G
ENST00000696560.1:c.895+29C>G (HLA-B)	ENSP00000512718.1:n.895+29C>G
ENST00000696561.1:c.895+29C>G (HLA-B)	ENSP00000512719.1:n.895+29C>G
ENST00000696562.1:c.895+29C>G (HLA-B)	ENSP00000512720.1:n.895+29C>G
ENST00000412585.7:c.895+29C>G (HLA-B) MANE Select	ENSP00000399168.2:n.895+29C>G
ENST00000640094.1:c.88+29C>G (HLA-B)	ENSP00000491275.1:n.88+29C>G
ENST00000412585.6:c.895+29C>G (HLA-B)	ENSP00000399168.2:n.895+29C>G
ENST00000463574.1:n.486+29C>G (HLA-B)
NM_005514.6:c.895+29C>G (HLA-B)	NP_005505.2:n.895+29C>G
NR_106951.1:n.29C>G (MIR6891)
XM_011514556.1:c.928+29C>G (HLA-B)	XP_011512858.1:n.928+29C>G
XM_011514557.1:c.895+29C>G (HLA-B)	XP_011512859.1:n.895+29C>G
XR_926175.1:n.1334+29C>G (HLA-B)
NM_005514.7:c.895+29C>G (HLA-B)	NP_005505.2:n.895+29C>G
NM_005514.8:c.895+29C>G (HLA-B) MANE Select	NP_005505.2:n.895+29C>G