Canonical Allele Identifier: CA2298939921
Gene: LINC00907 HGNC NCBI

Linked Data

dbSNP Id: rs1907319482

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42470543G>A , CM000680.2:g.42470543G>A GRCh38
NC_000018.9:g.40050508G>A , CM000680.1:g.40050508G>A GRCh37
NC_000018.8:g.38304506G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046174.2:n.872+15554G>A
NR_046454.1:n.652+15554G>A
NR_046455.1:n.489+15554G>A