Canonical Allele Identifier: CA1543249011
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs1739806435
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662235A>T , CM000667.2:g.44662235A>T GRCh38
NC_000005.9:g.44662337A>T , CM000667.1:g.44662337A>T GRCh37
NC_000005.8:g.44698094A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427699.2:n.92-3678T>A
XR_925983.1:n.71-3678T>A
Search 100 bp 5'
Search 100 bp 3'