Canonical Allele Identifier: CA2298939901
Gene: LINC00907 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42470473A= , CM000680.2:g.42470473A= GRCh38
NC_000018.9:g.40050438A= , CM000680.1:g.40050438A= GRCh37
NC_000018.8:g.38304436A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046174.2:n.872+15484A=
NR_046454.1:n.652+15484A=
NR_046455.1:n.489+15484A=