Canonical Allele Identifier: CA69736862

Gene: LINC00620

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.13701633G>T , CM000665.2:g.13701633G>T	GRCh38
NC_000003.11:g.13743132G>T , CM000665.1:g.13743132G>T	GRCh37
NC_000003.10:g.13718133G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_027103.1:n.217+13417G>T