Canonical Allele Identifier: CA85231859

Gene: LINC02045

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148217848C>A , CM000665.2:g.148217848C>A	GRCh38
NC_000003.11:g.147935635C>A , CM000665.1:g.147935635C>A	GRCh37
NC_000003.10:g.149418325C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_924565.1:n.86+2662G>T