Canonical Allele Identifier: CA1071107352

Gene: LINC02268

Linked Data

• dbSNP Id: rs1732973151
• gnomAD v3: 4-174106383-T-C
• gnomAD v4: 4-174106383-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.174106383T>C , CM000666.2:g.174106383T>C	GRCh38
NC_000004.11:g.175027534T>C , CM000666.1:g.175027534T>C	GRCh37
NC_000004.10:g.175264109T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_125896.1:n.276-8554A>G
XR_939484.1:n.877+18744T>C
XR_939485.1:n.877+18744T>C