Canonical Allele Identifier: CA811039867

Gene: LINC02224

Linked Data

• dbSNP Id: rs1417422035
• gnomAD v3: 5-44662237-C-A
• gnomAD v4: 5-44662237-C-A
• MyVariant Identifiers: chr5:g.44662339C>A (hg19) ; chr5:g.44662237C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44662237C>A , CM000667.2:g.44662237C>A	GRCh38
NC_000005.9:g.44662339C>A , CM000667.1:g.44662339C>A	GRCh37
NC_000005.8:g.44698096C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_427699.2:n.92-3680G>T
XR_925983.1:n.71-3680G>T