Canonical Allele Identifier: CA1180186316
Gene: LINC01725 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.83789052G>C , CM000663.2:g.83789052G>C GRCh38
NC_000001.10:g.84254735G>C , CM000663.1:g.84254735G>C GRCh37
NC_000001.9:g.84027323G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_119375.1:n.179-38753C>G