Canonical Allele Identifier: CA2596424752
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs1739810077
gnomAD v3: 5-44662605-C-A
gnomAD v4: 5-44662605-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662605C>A , CM000667.2:g.44662605C>A GRCh38
NC_000005.9:g.44662707C>A , CM000667.1:g.44662707C>A GRCh37
NC_000005.8:g.44698464C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427699.2:n.92-4048G>T
XR_925983.1:n.71-4048G>T
Search 100 bp 5'
Search 100 bp 3'