Canonical Allele Identifier: CA629642769
Gene: LINC00907 HGNC NCBI

Linked Data

dbSNP Id: rs1317384586

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42470318C>G , CM000680.2:g.42470318C>G GRCh38
NC_000018.9:g.40050283C>G , CM000680.1:g.40050283C>G GRCh37
NC_000018.8:g.38304281C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046174.2:n.872+15329C>G
NR_046454.1:n.652+15329C>G
NR_046455.1:n.489+15329C>G