Canonical Allele Identifier: CA14586071

Gene: LINC00907

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.42522676C>A , CM000680.2:g.42522676C>A	GRCh38
NC_000018.9:g.40102641C>A , CM000680.1:g.40102641C>A	GRCh37
NC_000018.8:g.38356639C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046174.2:n.873-52117C>A
NR_046454.1:n.703+6507C>A