Canonical Allele Identifier: CA118203153

Gene: LINC02224

Linked Data

• dbSNP Id: rs1043146788
• gnomAD v2: 5-44662541-G-A
• gnomAD v3: 5-44662439-G-A
• gnomAD v4: 5-44662439-G-A
• MyVariant Identifiers: chr5:g.44662541G>A (hg19) ; chr5:g.44662439G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44662439G>A , CM000667.2:g.44662439G>A	GRCh38
NC_000005.9:g.44662541G>A , CM000667.1:g.44662541G>A	GRCh37
NC_000005.8:g.44698298G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_427699.2:n.92-3882C>T
XR_925983.1:n.71-3882C>T