Canonical Allele Identifier: CA2708666552
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs1739806794

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662278G>T , CM000667.2:g.44662278G>T GRCh38
NC_000005.9:g.44662380G>T , CM000667.1:g.44662380G>T GRCh37
NC_000005.8:g.44698137G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427699.2:n.92-3721C>A
XR_925983.1:n.71-3721C>A