Canonical Allele Identifier: CA118203139

Gene: LINC02224

Linked Data

• dbSNP Id: rs973162682
• MyVariant Identifiers: chr5:g.44662446T>A (hg19) ; chr5:g.44662344T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44662344T>A , CM000667.2:g.44662344T>A	GRCh38
NC_000005.9:g.44662446T>A , CM000667.1:g.44662446T>A	GRCh37
NC_000005.8:g.44698203T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_427699.2:n.92-3787A>T
XR_925983.1:n.71-3787A>T