Canonical Allele Identifier: CA811040062
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs1370464227
MyVariant Identifiers: chr5:g.44662576A>G (hg19) chr5:g.44662474A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662474A>G , CM000667.2:g.44662474A>G GRCh38
NC_000005.9:g.44662576A>G , CM000667.1:g.44662576A>G GRCh37
NC_000005.8:g.44698333A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427699.2:n.92-3917T>C
XR_925983.1:n.71-3917T>C
Search 100 bp 5'
Search 100 bp 3'