Canonical Allele Identifier: CA2298939805
Gene: LINC00907 HGNC NCBI

Linked Data

dbSNP Id: rs1568130430

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42470262T>G , CM000680.2:g.42470262T>G GRCh38
NC_000018.9:g.40050227T>G , CM000680.1:g.40050227T>G GRCh37
NC_000018.8:g.38304225T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046174.2:n.872+15273T>G
NR_046454.1:n.652+15273T>G
NR_046455.1:n.489+15273T>G