Canonical Allele Identifier: CA472019284

Linked Data

MyVariant Identifiers: chr11:g.2194302T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2173072T>C , CM000673.2:g.2173072T>C GRCh38
NC_000011.9:g.2194302T>C , CM000673.1:g.2194302T>C GRCh37
NC_000011.8:g.2150878T>C NCBI36
NG_008128.1:g.3734A>G

Transcript Alleles

HGVS Amino-acid change
NR_039834.1:n.10T>C (MIR4686)
XM_011520335.2:c.-1286A>G (TH) XP_011518637.1:n.-1286A>G