Canonical Allele Identifier: CA472019282

Gene: MIR4686 TH

Linked Data

• gnomAD v4: 11-2173071-G-T
• MyVariant Identifiers: chr11:g.2194301G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2173071G>T , CM000673.2:g.2173071G>T	GRCh38
NC_000011.9:g.2194301G>T , CM000673.1:g.2194301G>T	GRCh37
NC_000011.8:g.2150877G>T	NCBI36
NG_008128.1:g.3735C>A

Transcript Alleles

HGVS	Amino-acid change
NR_039834.1:n.9G>T (MIR4686)
XM_011520335.2:c.-1285C>A (TH)	XP_011518637.1:n.-1285C>A