Canonical Allele Identifier: CA558962896

Gene: LINC02224

Linked Data

• dbSNP Id: rs1224742720
• gnomAD v2: 5-44662450-C-G
• gnomAD v3: 5-44662348-C-G
• gnomAD v4: 5-44662348-C-G
• MyVariant Identifiers: chr5:g.44662450C>G (hg19) ; chr5:g.44662348C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44662348C>G , CM000667.2:g.44662348C>G	GRCh38
NC_000005.9:g.44662450C>G , CM000667.1:g.44662450C>G	GRCh37
NC_000005.8:g.44698207C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_427699.2:n.92-3791G>C
XR_925983.1:n.71-3791G>C