Canonical Allele Identifier: CA2298939935
Gene: LINC00907 HGNC NCBI

Linked Data

dbSNP Id: rs1907320172

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42470563A>G , CM000680.2:g.42470563A>G GRCh38
NC_000018.9:g.40050528A>G , CM000680.1:g.40050528A>G GRCh37
NC_000018.8:g.38304526A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046174.2:n.872+15574A>G
NR_046454.1:n.652+15574A>G
NR_046455.1:n.489+15574A>G