Canonical Allele Identifier: CA754459778

Gene: LINC01965

Linked Data

• dbSNP Id: rs1232779555
• MyVariant Identifiers: chr2:g.104578420del (hg19) ; chr2:g.103961962del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.103961965del , CM000664.2:g.103961965del	GRCh38
NC_000002.11:g.104578423del , CM000664.1:g.104578423del	GRCh37
NC_000002.10:g.103944855del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001739621.1:n.178+87520del
XR_001739623.1:n.178+87520del