Canonical Allele Identifier: CA118203130
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs960601045
MyVariant Identifiers: chr5:g.44662255C>T (hg38)
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Genomic Alleles

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

Transcript Alleles

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