Canonical Allele Identifier: CA1543249048
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs1739806794

Genomic Alleles

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

Transcript Alleles

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