Canonical Allele Identifier: CA2298939931
Gene: LINC00907 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42470558T= , CM000680.2:g.42470558T= GRCh38
NC_000018.9:g.40050523T= , CM000680.1:g.40050523T= GRCh37
NC_000018.8:g.38304521T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046174.2:n.872+15569T=
NR_046454.1:n.652+15569T=
NR_046455.1:n.489+15569T=