Canonical Allele Identifier: CA754459818

Gene: LINC01965

Linked Data

• dbSNP Id: rs1326143349
• gnomAD v3: 2-103962070-C-T
• gnomAD v4: 2-103962070-C-T
• MyVariant Identifiers: chr2:g.104578528C>T (hg19) ; chr2:g.103962070C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.103962070C>T , CM000664.2:g.103962070C>T	GRCh38
NC_000002.11:g.104578528C>T , CM000664.1:g.104578528C>T	GRCh37
NC_000002.10:g.103944960C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001739621.1:n.178+87625C>T
XR_001739623.1:n.178+87625C>T