Canonical Allele Identifier: CA53064924

Gene: LINC01965

Linked Data

• dbSNP Id: rs192704753
• gnomAD v3: 2-103962194-A-G
• gnomAD v4: 2-103962194-A-G
• MyVariant Identifiers: chr2:g.104578652A>G (hg19) ; chr2:g.103962194A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.103962194A>G , CM000664.2:g.103962194A>G	GRCh38
NC_000002.11:g.104578652A>G , CM000664.1:g.104578652A>G	GRCh37
NC_000002.10:g.103945084A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001739621.1:n.178+87749A>G
XR_001739623.1:n.178+87749A>G