Canonical Allele Identifier: CA754459855

Gene: LINC01965

Linked Data

• dbSNP Id: rs1487628786
• gnomAD v3: 2-103962160-A-G
• gnomAD v4: 2-103962160-A-G
• MyVariant Identifiers: chr2:g.104578618A>G (hg19) ; chr2:g.103962160A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.103962160A>G , CM000664.2:g.103962160A>G	GRCh38
NC_000002.11:g.104578618A>G , CM000664.1:g.104578618A>G	GRCh37
NC_000002.10:g.103945050A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001739621.1:n.178+87715A>G
XR_001739623.1:n.178+87715A>G