Canonical Allele Identifier: CA989645799
Gene: LINC00907 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42470394A>T , CM000680.2:g.42470394A>T GRCh38
NC_000018.9:g.40050359A>T , CM000680.1:g.40050359A>T GRCh37
NC_000018.8:g.38304357A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046174.2:n.872+15405A>T
NR_046454.1:n.652+15405A>T
NR_046455.1:n.489+15405A>T