Canonical Allele Identifier: CA811039922

Gene: LINC02224

Linked Data

• dbSNP Id: rs1417319122
• gnomAD v3: 5-44662328-TG-T
• gnomAD v4: 5-44662328-TG-T
• MyVariant Identifiers: chr5:g.44662431del (hg19) ; chr5:g.44662329del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44662330del , CM000667.2:g.44662330del	GRCh38
NC_000005.9:g.44662432del , CM000667.1:g.44662432del	GRCh37
NC_000005.8:g.44698189del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_427699.2:n.92-3772del
XR_925983.1:n.71-3772del