Canonical Allele Identifier: CA1752145313
Gene: RARRES2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150339587A= , CM000669.2:g.150339587A= GRCh38
NC_000007.13:g.150036676A= , CM000669.1:g.150036676A= GRCh37
NC_000007.12:g.149667609A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000223271.8:c.280-506T= MANE Select ENSP00000223271.3:n.280-506T=
ENST00000223271.7:c.280-506T= ENSP00000223271.3:n.280-506T=
ENST00000466675.5:c.280-506T= ENSP00000418009.1:n.280-506T=
ENST00000467793.5:c.280-506T= ENSP00000417669.1:n.280-506T=
ENST00000478771.2:n.1562-506T=
ENST00000482669.1:c.280-506T= ENSP00000418483.1:n.280-506T=
NM_002889.3:c.280-506T= NP_002880.1:n.280-506T=
XM_017012491.1:c.280-506T= XP_016867980.1:n.280-506T=
NM_002889.4:c.280-506T= MANE Select NP_002880.1:n.280-506T=