Canonical Allele Identifier: CA118203166
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs760472304
gnomAD v2: 5-44662724-C-A
gnomAD v3: 5-44662622-C-A
gnomAD v4: 5-44662622-C-A
MyVariant Identifiers: chr5:g.44662724C>A (hg19) chr5:g.44662622C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662622C>A , CM000667.2:g.44662622C>A GRCh38
NC_000005.9:g.44662724C>A , CM000667.1:g.44662724C>A GRCh37
NC_000005.8:g.44698481C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427699.2:n.92-4065G>T
XR_925983.1:n.71-4065G>T
Search 100 bp 5'
Search 100 bp 3'