Canonical Allele Identifier: CA2298939919
Gene: LINC00907 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42470542A= , CM000680.2:g.42470542A= GRCh38
NC_000018.9:g.40050507A= , CM000680.1:g.40050507A= GRCh37
NC_000018.8:g.38304505A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046174.2:n.872+15553A=
NR_046454.1:n.652+15553A=
NR_046455.1:n.489+15553A=