Canonical Allele Identifier: CA299441722
Gene: LINC00907 HGNC NCBI

Linked Data

dbSNP Id: rs745357566

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42470258_42470264del , CM000680.2:g.42470258_42470264del GRCh38
NC_000018.9:g.40050223_40050229del , CM000680.1:g.40050223_40050229del GRCh37
NC_000018.8:g.38304221_38304227del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046174.2:n.872+15269_872+15275del
NR_046454.1:n.652+15269_652+15275del
NR_046455.1:n.489+15269_489+15275del