Canonical Allele Identifier: CA558962908

Gene: LINC02224

Linked Data

• dbSNP Id: rs1477765121
• gnomAD v2: 5-44662534-C-T
• gnomAD v3: 5-44662432-C-T
• gnomAD v4: 5-44662432-C-T
• MyVariant Identifiers: chr5:g.44662534C>T (hg19) ; chr5:g.44662432C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44662432C>T , CM000667.2:g.44662432C>T	GRCh38
NC_000005.9:g.44662534C>T , CM000667.1:g.44662534C>T	GRCh37
NC_000005.8:g.44698291C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_427699.2:n.92-3875G>A
XR_925983.1:n.71-3875G>A