Canonical Allele Identifier: CA989645826
Gene: LINC00907 HGNC NCBI

Linked Data

dbSNP Id: rs1907317456

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42470425_42470427del , CM000680.2:g.42470425_42470427del GRCh38
NC_000018.9:g.40050390_40050392del , CM000680.1:g.40050390_40050392del GRCh37
NC_000018.8:g.38304388_38304390del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046174.2:n.872+15436_872+15438del
NR_046454.1:n.652+15436_652+15438del
NR_046455.1:n.489+15436_489+15438del