Canonical Allele Identifier: CA811039873
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs960601045
gnomAD v3: 5-44662255-C-G
gnomAD v4: 5-44662255-C-G
MyVariant Identifiers: chr5:g.44662357C>G (hg19) chr5:g.44662255C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662255C>G , CM000667.2:g.44662255C>G GRCh38
NC_000005.9:g.44662357C>G , CM000667.1:g.44662357C>G GRCh37
NC_000005.8:g.44698114C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427699.2:n.92-3698G>C
XR_925983.1:n.71-3698G>C
Search 100 bp 5'
Search 100 bp 3'