Canonical Allele Identifier: CA299441725
Gene: LINC00907 HGNC NCBI

Linked Data

dbSNP Id: rs957608512

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42470265T>C , CM000680.2:g.42470265T>C GRCh38
NC_000018.9:g.40050230T>C , CM000680.1:g.40050230T>C GRCh37
NC_000018.8:g.38304228T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046174.2:n.872+15276T>C
NR_046454.1:n.652+15276T>C
NR_046455.1:n.489+15276T>C