Canonical Allele Identifier: CA989645758
Gene: LINC00907 HGNC NCBI

Linked Data

dbSNP Id: rs1907311991

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42470255G>T , CM000680.2:g.42470255G>T GRCh38
NC_000018.9:g.40050220G>T , CM000680.1:g.40050220G>T GRCh37
NC_000018.8:g.38304218G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046174.2:n.872+15266G>T
NR_046454.1:n.652+15266G>T
NR_046455.1:n.489+15266G>T