Canonical Allele Identifier: CA118203146
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs911805585
gnomAD v3: 5-44662400-G-C
gnomAD v4: 5-44662400-G-C
MyVariant Identifiers: chr5:g.44662502G>C (hg19) chr5:g.44662400G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662400G>C , CM000667.2:g.44662400G>C GRCh38
NC_000005.9:g.44662502G>C , CM000667.1:g.44662502G>C GRCh37
NC_000005.8:g.44698259G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427699.2:n.92-3843C>G
XR_925983.1:n.71-3843C>G
Search 100 bp 5'
Search 100 bp 3'