Canonical Allele Identifier: CA2298939870
Gene: LINC00907 HGNC NCBI

Linked Data

dbSNP Id: rs1599193837

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42470380T>A , CM000680.2:g.42470380T>A GRCh38
NC_000018.9:g.40050345T>A , CM000680.1:g.40050345T>A GRCh37
NC_000018.8:g.38304343T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046174.2:n.872+15391T>A
NR_046454.1:n.652+15391T>A
NR_046455.1:n.489+15391T>A