Canonical Allele Identifier: CA2298939810
Gene: LINC00907 HGNC NCBI

Linked Data

dbSNP Id: rs1907312632

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42470271G>A , CM000680.2:g.42470271G>A GRCh38
NC_000018.9:g.40050236G>A , CM000680.1:g.40050236G>A GRCh37
NC_000018.8:g.38304234G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046174.2:n.872+15282G>A
NR_046454.1:n.652+15282G>A
NR_046455.1:n.489+15282G>A