Canonical Allele Identifier: CA989645808
Gene: LINC00907 HGNC NCBI

Linked Data

dbSNP Id: rs1907317179

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42470408C>A , CM000680.2:g.42470408C>A GRCh38
NC_000018.9:g.40050373C>A , CM000680.1:g.40050373C>A GRCh37
NC_000018.8:g.38304371C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046174.2:n.872+15419C>A
NR_046454.1:n.652+15419C>A
NR_046455.1:n.489+15419C>A