Canonical Allele Identifier: CA558962890
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs1414392207
gnomAD v2: 5-44662414-C-T
gnomAD v3: 5-44662312-C-T
gnomAD v4: 5-44662312-C-T
MyVariant Identifiers: chr5:g.44662414C>T (hg19) chr5:g.44662312C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662312C>T , CM000667.2:g.44662312C>T GRCh38
NC_000005.9:g.44662414C>T , CM000667.1:g.44662414C>T GRCh37
NC_000005.8:g.44698171C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427699.2:n.92-3755G>A
XR_925983.1:n.71-3755G>A
Search 100 bp 5'
Search 100 bp 3'