Canonical Allele Identifier: CA2298939913
Gene: LINC00907 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42470524C= , CM000680.2:g.42470524C= GRCh38
NC_000018.9:g.40050489C= , CM000680.1:g.40050489C= GRCh37
NC_000018.8:g.38304487C= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046174.2:n.872+15535C=
NR_046454.1:n.652+15535C=
NR_046455.1:n.489+15535C=