Canonical Allele Identifier: CA811039815

Gene: LINC02224

Linked Data

• dbSNP Id: rs1191996347
• MyVariant Identifiers: chr5:g.44662251G>A (hg19) ; chr5:g.44662149G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44662149G>A , CM000667.2:g.44662149G>A	GRCh38
NC_000005.9:g.44662251G>A , CM000667.1:g.44662251G>A	GRCh37
NC_000005.8:g.44698008G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_427699.2:n.92-3592C>T
XR_925983.1:n.71-3592C>T