Canonical Allele Identifier: CA2298939849
Gene: LINC00907 HGNC NCBI

Linked Data

dbSNP Id: rs1907314654

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42470345dup , CM000680.2:g.42470345dup GRCh38
NC_000018.9:g.40050310dup , CM000680.1:g.40050310dup GRCh37
NC_000018.8:g.38304308dup NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046174.2:n.872+15356dup
NR_046454.1:n.652+15356dup
NR_046455.1:n.489+15356dup