Canonical Allele Identifier: CA629642772
Gene: LINC00907 HGNC NCBI

Linked Data

dbSNP Id: rs1293361034

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42470350C>G , CM000680.2:g.42470350C>G GRCh38
NC_000018.9:g.40050315C>G , CM000680.1:g.40050315C>G GRCh37
NC_000018.8:g.38304313C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046174.2:n.872+15361C>G
NR_046454.1:n.652+15361C>G
NR_046455.1:n.489+15361C>G