Canonical Allele Identifier: CA118203149

Gene: LINC02224

Linked Data

• dbSNP Id: rs896467703
• gnomAD v3: 5-44662416-A-C
• gnomAD v4: 5-44662416-A-C
• MyVariant Identifiers: chr5:g.44662518A>C (hg19) ; chr5:g.44662416A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44662416A>C , CM000667.2:g.44662416A>C	GRCh38
NC_000005.9:g.44662518A>C , CM000667.1:g.44662518A>C	GRCh37
NC_000005.8:g.44698275A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_427699.2:n.92-3859T>G
XR_925983.1:n.71-3859T>G