Canonical Allele Identifier: CA12962693

Gene: LINC02937

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91090533G>T , CM000671.2:g.91090533G>T	GRCh38
NC_000009.11:g.93852815G>T , CM000671.1:g.93852815G>T	GRCh37
NC_000009.10:g.92892636G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001746830.2:n.13193+7889C>A