Canonical Allele Identifier: CA2298939820
Gene: LINC00907 HGNC NCBI

Linked Data

dbSNP Id: rs1907313034

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42470286G>C , CM000680.2:g.42470286G>C GRCh38
NC_000018.9:g.40050251G>C , CM000680.1:g.40050251G>C GRCh37
NC_000018.8:g.38304249G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046174.2:n.872+15297G>C
NR_046454.1:n.652+15297G>C
NR_046455.1:n.489+15297G>C