Canonical Allele Identifier: CA919972775
Gene: LINC00907 HGNC NCBI

Linked Data

dbSNP Id: rs1568130421

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42470252_42470257del , CM000680.2:g.42470252_42470257del GRCh38
NC_000018.9:g.40050217_40050222del , CM000680.1:g.40050217_40050222del GRCh37
NC_000018.8:g.38304215_38304220del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046174.2:n.872+15263_872+15268del
NR_046454.1:n.652+15263_652+15268del
NR_046455.1:n.489+15263_489+15268del