Canonical Allele Identifier: CA53064896

Gene: LINC01965

Linked Data

• dbSNP Id: rs918571130
• gnomAD v3: 2-103962050-A-G
• gnomAD v4: 2-103962050-A-G
• MyVariant Identifiers: chr2:g.104578508A>G (hg19) ; chr2:g.103962050A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.103962050A>G , CM000664.2:g.103962050A>G	GRCh38
NC_000002.11:g.104578508A>G , CM000664.1:g.104578508A>G	GRCh37
NC_000002.10:g.103944940A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001739621.1:n.178+87605A>G
XR_001739623.1:n.178+87605A>G