Canonical Allele Identifier: CA754459805

Gene: LINC01965

Linked Data

• dbSNP Id: rs1293166236
• gnomAD v3: 2-103962055-A-C
• gnomAD v4: 2-103962055-A-C
• MyVariant Identifiers: chr2:g.104578513A>C (hg19) ; chr2:g.103962055A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.103962055A>C , CM000664.2:g.103962055A>C	GRCh38
NC_000002.11:g.104578513A>C , CM000664.1:g.104578513A>C	GRCh37
NC_000002.10:g.103944945A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001739621.1:n.178+87610A>C
XR_001739623.1:n.178+87610A>C