Canonical Allele Identifier: CA1543249040
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs1739806723

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662270A>C , CM000667.2:g.44662270A>C GRCh38
NC_000005.9:g.44662372A>C , CM000667.1:g.44662372A>C GRCh37
NC_000005.8:g.44698129A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427699.2:n.92-3713T>G
XR_925983.1:n.71-3713T>G