Canonical Allele Identifier: CA1075652740
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs1739806387
gnomAD v3: 5-44662233-A-T
gnomAD v4: 5-44662233-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662233A>T , CM000667.2:g.44662233A>T GRCh38
NC_000005.9:g.44662335A>T , CM000667.1:g.44662335A>T GRCh37
NC_000005.8:g.44698092A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427699.2:n.92-3676T>A
XR_925983.1:n.71-3676T>A