Canonical Allele Identifier: CA114292532

Gene: LINC02213

Linked Data

• dbSNP Id: rs755668582
• gnomAD v3: 5-10512508-A-C
• gnomAD v4: 5-10512508-A-C
• MyVariant Identifiers: chr5:g.10512620A>C (hg19) ; chr5:g.10512508A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10512508A>C , CM000667.2:g.10512508A>C	GRCh38
NC_000005.9:g.10512620A>C , CM000667.1:g.10512620A>C	GRCh37
NC_000005.8:g.10565620A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_134289.1:n.330-5933T>G