Canonical Allele Identifier: CA811039994
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs1466384348
MyVariant Identifiers: chr5:g.44662500C>A (hg19) chr5:g.44662398C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662398C>A , CM000667.2:g.44662398C>A GRCh38
NC_000005.9:g.44662500C>A , CM000667.1:g.44662500C>A GRCh37
NC_000005.8:g.44698257C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427699.2:n.92-3841G>T
XR_925983.1:n.71-3841G>T
Search 100 bp 5'
Search 100 bp 3'