Canonical Allele Identifier: CA1075652839
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs1739807531
gnomAD v3: 5-44662342-A-G
gnomAD v4: 5-44662342-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662342A>G , CM000667.2:g.44662342A>G GRCh38
NC_000005.9:g.44662444A>G , CM000667.1:g.44662444A>G GRCh37
NC_000005.8:g.44698201A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427699.2:n.92-3785T>C
XR_925983.1:n.71-3785T>C