Canonical Allele Identifier: CA118203158
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs184502931
gnomAD v2: 5-44662572-A-G
gnomAD v3: 5-44662470-A-G
gnomAD v4: 5-44662470-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662470A>G , CM000667.2:g.44662470A>G GRCh38
NC_000005.9:g.44662572A>G , CM000667.1:g.44662572A>G GRCh37
NC_000005.8:g.44698329A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427699.2:n.92-3913T>C
XR_925983.1:n.71-3913T>C