Canonical Allele Identifier: CA1543248966
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs1739805389
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662175A>G , CM000667.2:g.44662175A>G GRCh38
NC_000005.9:g.44662277A>G , CM000667.1:g.44662277A>G GRCh37
NC_000005.8:g.44698034A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427699.2:n.92-3618T>C
XR_925983.1:n.71-3618T>C
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Search 100 bp 3'