Canonical Allele Identifier: CA2298939801
Gene: LINC00907 HGNC NCBI

Linked Data

dbSNP Id: rs1907312058

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42470258A>G , CM000680.2:g.42470258A>G GRCh38
NC_000018.9:g.40050223A>G , CM000680.1:g.40050223A>G GRCh37
NC_000018.8:g.38304221A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046174.2:n.872+15269A>G
NR_046454.1:n.652+15269A>G
NR_046455.1:n.489+15269A>G