Canonical Allele Identifier: CA989645766
Gene: LINC00907 HGNC NCBI

Linked Data

dbSNP Id: rs1907313297

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42470290T>A , CM000680.2:g.42470290T>A GRCh38
NC_000018.9:g.40050255T>A , CM000680.1:g.40050255T>A GRCh37
NC_000018.8:g.38304253T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046174.2:n.872+15301T>A
NR_046454.1:n.652+15301T>A
NR_046455.1:n.489+15301T>A