Canonical Allele Identifier: CA472019254
Gene: MIR4686 HGNC NCBI
TH HGNC NCBI

Linked Data

gnomAD v4: 11-2173064-G-A
MyVariant Identifiers: chr11:g.2194294G>A (hg19)
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Genomic Alleles

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

Transcript Alleles

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