Canonical Allele Identifier: CA1948013599

Genomic Alleles

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

Transcript Alleles

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