Canonical Allele Identifier: CA754459809

Gene: LINC01965

Linked Data

• dbSNP Id: rs1465145484
• gnomAD v3: 2-103962061-T-C
• gnomAD v4: 2-103962061-T-C
• MyVariant Identifiers: chr2:g.104578519T>C (hg19) ; chr2:g.103962061T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.103962061T>C , CM000664.2:g.103962061T>C	GRCh38
NC_000002.11:g.104578519T>C , CM000664.1:g.104578519T>C	GRCh37
NC_000002.10:g.103944951T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001739621.1:n.178+87616T>C
XR_001739623.1:n.178+87616T>C