Canonical Allele Identifier: CA791203245

Gene: LINC02268

Linked Data

• dbSNP Id: rs1302069525
• MyVariant Identifiers: chr4:g.175027441T>C (hg19) ; chr4:g.174106290T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.174106290T>C , CM000666.2:g.174106290T>C	GRCh38
NC_000004.11:g.175027441T>C , CM000666.1:g.175027441T>C	GRCh37
NC_000004.10:g.175264016T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_125896.1:n.276-8461A>G
XR_939484.1:n.877+18651T>C
XR_939485.1:n.877+18651T>C