Canonical Allele Identifier: CA53064921

Gene: LINC01965

Linked Data

• dbSNP Id: rs893468314
• MyVariant Identifiers: chr2:g.104578636T>C (hg19) ; chr2:g.103962178T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.103962178T>C , CM000664.2:g.103962178T>C	GRCh38
NC_000002.11:g.104578636T>C , CM000664.1:g.104578636T>C	GRCh37
NC_000002.10:g.103945068T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001739621.1:n.178+87733T>C
XR_001739623.1:n.178+87733T>C