Canonical Allele Identifier: CA111096865

Gene: LINC02268

Linked Data

• dbSNP Id: rs1052506312
• gnomAD v3: 4-174106375-G-T
• gnomAD v4: 4-174106375-G-T
• MyVariant Identifiers: chr4:g.175027526G>T (hg19) ; chr4:g.174106375G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.174106375G>T , CM000666.2:g.174106375G>T	GRCh38
NC_000004.11:g.175027526G>T , CM000666.1:g.175027526G>T	GRCh37
NC_000004.10:g.175264101G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_125896.1:n.276-8546C>A
XR_939484.1:n.877+18736G>T
XR_939485.1:n.877+18736G>T