Canonical Allele Identifier: CA2298939897
Gene: LINC00907 HGNC NCBI

Linked Data

dbSNP Id: rs8093311

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42470463C>G , CM000680.2:g.42470463C>G GRCh38
NC_000018.9:g.40050428C>G , CM000680.1:g.40050428C>G GRCh37
NC_000018.8:g.38304426C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046174.2:n.872+15474C>G
NR_046454.1:n.652+15474C>G
NR_046455.1:n.489+15474C>G