Canonical Allele Identifier: CA118203125
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs779698750
MyVariant Identifiers: chr5:g.44662313C>G (hg19) chr5:g.44662211C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662211C>G , CM000667.2:g.44662211C>G GRCh38
NC_000005.9:g.44662313C>G , CM000667.1:g.44662313C>G GRCh37
NC_000005.8:g.44698070C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427699.2:n.92-3654G>C
XR_925983.1:n.71-3654G>C
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