Canonical Allele Identifier: CA118203138

Gene: LINC02224

Linked Data

• dbSNP Id: rs13153596
• MyVariant Identifiers: chr5:g.44662433A>G (hg19) ; chr5:g.44662331A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44662331A>G , CM000667.2:g.44662331A>G	GRCh38
NC_000005.9:g.44662433A>G , CM000667.1:g.44662433A>G	GRCh37
NC_000005.8:g.44698190A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_427699.2:n.92-3774T>C
XR_925983.1:n.71-3774T>C