Canonical Allele Identifier: CA989645845
Gene: LINC00907 HGNC NCBI

Linked Data

dbSNP Id: rs1907318522

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42470491A>C , CM000680.2:g.42470491A>C GRCh38
NC_000018.9:g.40050456A>C , CM000680.1:g.40050456A>C GRCh37
NC_000018.8:g.38304454A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046174.2:n.872+15502A>C
NR_046454.1:n.652+15502A>C
NR_046455.1:n.489+15502A>C