Canonical Allele Identifier: CA811039971
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs1272041419
MyVariant Identifiers: chr5:g.44662479A>T (hg19) chr5:g.44662377A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662377A>T , CM000667.2:g.44662377A>T GRCh38
NC_000005.9:g.44662479A>T , CM000667.1:g.44662479A>T GRCh37
NC_000005.8:g.44698236A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427699.2:n.92-3820T>A
XR_925983.1:n.71-3820T>A
Search 100 bp 5'
Search 100 bp 3'