Canonical Allele Identifier: CA16591900

Gene: LINC01697

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.28102877C>T , CM000683.2:g.28102877C>T	GRCh38
NC_000021.8:g.29475196C>T , CM000683.1:g.29475196C>T	GRCh37
NC_000021.7:g.28397067C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_126010.1:n.344+108C>T
NR_126011.1:n.501C>T