Canonical Allele Identifier: CA2596424743
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs2111567690
gnomAD v3: 5-44662316-A-G
gnomAD v4: 5-44662316-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662316A>G , CM000667.2:g.44662316A>G GRCh38
NC_000005.9:g.44662418A>G , CM000667.1:g.44662418A>G GRCh37
NC_000005.8:g.44698175A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427699.2:n.92-3759T>C
XR_925983.1:n.71-3759T>C