Canonical Allele Identifier: CA2298965278
Gene: LINC00907 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42525692T= , CM000680.2:g.42525692T= GRCh38
NC_000018.9:g.40105657T= , CM000680.1:g.40105657T= GRCh37
NC_000018.8:g.38359655T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046174.2:n.873-49101T=
NR_046454.1:n.704-7427T=