Canonical Allele Identifier: CA754459853

Gene: LINC01965

Linked Data

• dbSNP Id: rs1193305782
• gnomAD v3: 2-103962155-A-G
• gnomAD v4: 2-103962155-A-G
• MyVariant Identifiers: chr2:g.104578613A>G (hg19) ; chr2:g.103962155A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.103962155A>G , CM000664.2:g.103962155A>G	GRCh38
NC_000002.11:g.104578613A>G , CM000664.1:g.104578613A>G	GRCh37
NC_000002.10:g.103945045A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001739621.1:n.178+87710A>G
XR_001739623.1:n.178+87710A>G