Canonical Allele Identifier: CA1075652814
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs556607633
gnomAD v3: 5-44662304-A-G
gnomAD v4: 5-44662304-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662304A>G , CM000667.2:g.44662304A>G GRCh38
NC_000005.9:g.44662406A>G , CM000667.1:g.44662406A>G GRCh37
NC_000005.8:g.44698163A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427699.2:n.92-3747T>C
XR_925983.1:n.71-3747T>C