Canonical Allele Identifier: CA2303180316
Gene: LINC01630 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.51492510C>G , CM000680.2:g.51492510C>G GRCh38
NC_000018.9:g.49018880C>G , CM000680.1:g.49018880C>G GRCh37
NC_000018.8:g.47272878C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040074.1:n.217-68083C>G