Canonical Allele Identifier: CA558962895

Gene: LINC02224

Linked Data

• dbSNP Id: rs1345768334
• gnomAD v2: 5-44662431-G-C
• gnomAD v3: 5-44662329-G-C
• gnomAD v4: 5-44662329-G-C
• MyVariant Identifiers: chr5:g.44662431G>C (hg19) ; chr5:g.44662329G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44662329G>C , CM000667.2:g.44662329G>C	GRCh38
NC_000005.9:g.44662431G>C , CM000667.1:g.44662431G>C	GRCh37
NC_000005.8:g.44698188G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_427699.2:n.92-3772C>G
XR_925983.1:n.71-3772C>G