Canonical Allele Identifier: CA2298939838
Gene: LINC00907 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42470318C= , CM000680.2:g.42470318C= GRCh38
NC_000018.9:g.40050283C= , CM000680.1:g.40050283C= GRCh37
NC_000018.8:g.38304281C= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046174.2:n.872+15329C=
NR_046454.1:n.652+15329C=
NR_046455.1:n.489+15329C=