Canonical Allele Identifier: CA472019260
Gene: MIR4686 HGNC NCBI
TH HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.2194296T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2173066T>A , CM000673.2:g.2173066T>A GRCh38
NC_000011.9:g.2194296T>A , CM000673.1:g.2194296T>A GRCh37
NC_000011.8:g.2150872T>A NCBI36
NG_008128.1:g.3740A>T

Transcript Alleles

HGVS Amino-acid change
NR_039834.1:n.4T>A (MIR4686)
XM_011520335.2:c.-1280A>T (TH) XP_011518637.1:n.-1280A>T
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