Canonical Allele Identifier: CA12815221

Gene: LINC01607

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.79779234A>G , CM000670.2:g.79779234A>G	GRCh38
NC_000008.10:g.80691469A>G , CM000670.1:g.80691469A>G	GRCh37
NC_000008.9:g.80854024A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110954.1:n.437-7612T>C
NR_125410.1:n.139-774A>G