Canonical Allele Identifier: CA754459826

Gene: LINC01965

Linked Data

• dbSNP Id: rs1433835674
• MyVariant Identifiers: chr2:g.104578565C>T (hg19) ; chr2:g.103962107C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.103962107C>T , CM000664.2:g.103962107C>T	GRCh38
NC_000002.11:g.104578565C>T , CM000664.1:g.104578565C>T	GRCh37
NC_000002.10:g.103944997C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001739621.1:n.178+87662C>T
XR_001739623.1:n.178+87662C>T