Canonical Allele Identifier: CA835178450
Gene: RARRES2 HGNC NCBI

Linked Data

dbSNP Id: rs1419679690

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150339588G>T , CM000669.2:g.150339588G>T GRCh38
NC_000007.13:g.150036677G>T , CM000669.1:g.150036677G>T GRCh37
NC_000007.12:g.149667610G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000223271.8:c.280-507C>A MANE Select ENSP00000223271.3:n.280-507C>A
ENST00000223271.7:c.280-507C>A ENSP00000223271.3:n.280-507C>A
ENST00000466675.5:c.280-507C>A ENSP00000418009.1:n.280-507C>A
ENST00000467793.5:c.280-507C>A ENSP00000417669.1:n.280-507C>A
ENST00000478771.2:n.1562-507C>A
ENST00000482669.1:c.280-507C>A ENSP00000418483.1:n.280-507C>A
NM_002889.3:c.280-507C>A NP_002880.1:n.280-507C>A
XM_017012491.1:c.280-507C>A XP_016867980.1:n.280-507C>A
NM_002889.4:c.280-507C>A MANE Select NP_002880.1:n.280-507C>A