Canonical Allele Identifier: CA989645807
Gene: LINC00907 HGNC NCBI

Linked Data

dbSNP Id: rs1907316991

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42470402A>T , CM000680.2:g.42470402A>T GRCh38
NC_000018.9:g.40050367A>T , CM000680.1:g.40050367A>T GRCh37
NC_000018.8:g.38304365A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046174.2:n.872+15413A>T
NR_046454.1:n.652+15413A>T
NR_046455.1:n.489+15413A>T