Canonical Allele Identifier: CA472019255
Gene: MIR4686 HGNC NCBI
TH HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.2194294G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2173064G>C , CM000673.2:g.2173064G>C GRCh38
NC_000011.9:g.2194294G>C , CM000673.1:g.2194294G>C GRCh37
NC_000011.8:g.2150870G>C NCBI36
NG_008128.1:g.3742C>G

Transcript Alleles

HGVS Amino-acid change
NR_039834.1:n.2G>C (MIR4686)
XM_011520335.2:c.-1278C>G (TH) XP_011518637.1:n.-1278C>G
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