Canonical Allele Identifier: CA118203137

Gene: LINC02224

Linked Data

• dbSNP Id: rs779050950
• gnomAD v2: 5-44662427-C-G
• gnomAD v3: 5-44662325-C-G
• gnomAD v4: 5-44662325-C-G
• MyVariant Identifiers: chr5:g.44662427C>G (hg19) ; chr5:g.44662325C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44662325C>G , CM000667.2:g.44662325C>G	GRCh38
NC_000005.9:g.44662427C>G , CM000667.1:g.44662427C>G	GRCh37
NC_000005.8:g.44698184C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_427699.2:n.92-3768G>C
XR_925983.1:n.71-3768G>C