Canonical Allele Identifier: CA558962905
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs1262670124
gnomAD v2: 5-44662497-T-C
gnomAD v3: 5-44662395-T-C
gnomAD v4: 5-44662395-T-C
MyVariant Identifiers: chr5:g.44662497T>C (hg19) chr5:g.44662395T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662395T>C , CM000667.2:g.44662395T>C GRCh38
NC_000005.9:g.44662497T>C , CM000667.1:g.44662497T>C GRCh37
NC_000005.8:g.44698254T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427699.2:n.92-3838A>G
XR_925983.1:n.71-3838A>G
Search 100 bp 5'
Search 100 bp 3'