Canonical Allele Identifier: CA28744445

Gene: LINC01768

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109896858C>A , CM000663.2:g.109896858C>A	GRCh38
NC_000001.10:g.110439480C>A , CM000663.1:g.110439480C>A	GRCh37
NC_000001.9:g.110241003C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001738180.2:n.846-8849C>A