Canonical Allele Identifier: CA556641262

Gene: LINC02268

Linked Data

• dbSNP Id: rs1157288647
• gnomAD v2: 4-175027555-T-C
• gnomAD v3: 4-174106404-T-C
• gnomAD v4: 4-174106404-T-C
• MyVariant Identifiers: chr4:g.175027555T>C (hg19) ; chr4:g.174106404T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.174106404T>C , CM000666.2:g.174106404T>C	GRCh38
NC_000004.11:g.175027555T>C , CM000666.1:g.175027555T>C	GRCh37
NC_000004.10:g.175264130T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_125896.1:n.276-8575A>G
XR_939484.1:n.877+18765T>C
XR_939485.1:n.877+18765T>C