Canonical Allele Identifier: CA118203136

Gene: LINC02224

Linked Data

• dbSNP Id: rs576471954
• gnomAD v2: 5-44662425-C-A
• gnomAD v3: 5-44662323-C-A
• gnomAD v4: 5-44662323-C-A
• MyVariant Identifiers: chr5:g.44662425C>A (hg19) ; chr5:g.44662323C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44662323C>A , CM000667.2:g.44662323C>A	GRCh38
NC_000005.9:g.44662425C>A , CM000667.1:g.44662425C>A	GRCh37
NC_000005.8:g.44698182C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_427699.2:n.92-3766G>T
XR_925983.1:n.71-3766G>T