Canonical Allele Identifier: CA118203142
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs931669059
gnomAD v3: 5-44662373-C-T
gnomAD v4: 5-44662373-C-T
MyVariant Identifiers: chr5:g.44662475C>T (hg19) chr5:g.44662373C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662373C>T , CM000667.2:g.44662373C>T GRCh38
NC_000005.9:g.44662475C>T , CM000667.1:g.44662475C>T GRCh37
NC_000005.8:g.44698232C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427699.2:n.92-3816G>A
XR_925983.1:n.71-3816G>A
Search 100 bp 5'
Search 100 bp 3'