Canonical Allele Identifier: CA472019271

Gene: MIR4686 TH

Linked Data

• MyVariant Identifiers: chr11:g.2194299C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2173069C>G , CM000673.2:g.2173069C>G	GRCh38
NC_000011.9:g.2194299C>G , CM000673.1:g.2194299C>G	GRCh37
NC_000011.8:g.2150875C>G	NCBI36
NG_008128.1:g.3737G>C

Transcript Alleles

HGVS	Amino-acid change
NR_039834.1:n.7C>G (MIR4686)
XM_011520335.2:c.-1283G>C (TH)	XP_011518637.1:n.-1283G>C