Canonical Allele Identifier: CA1752145288
Gene: RARRES2 HGNC NCBI

Linked Data

dbSNP Id: rs1585053271

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150339534T>A , CM000669.2:g.150339534T>A GRCh38
NC_000007.13:g.150036623T>A , CM000669.1:g.150036623T>A GRCh37
NC_000007.12:g.149667556T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000223271.8:c.280-453A>T MANE Select ENSP00000223271.3:n.280-453A>T
ENST00000223271.7:c.280-453A>T ENSP00000223271.3:n.280-453A>T
ENST00000466675.5:c.280-453A>T ENSP00000418009.1:n.280-453A>T
ENST00000467793.5:c.280-453A>T ENSP00000417669.1:n.280-453A>T
ENST00000478771.2:n.1562-453A>T
ENST00000482669.1:c.280-453A>T ENSP00000418483.1:n.280-453A>T
NM_002889.3:c.280-453A>T NP_002880.1:n.280-453A>T
XM_017012491.1:c.280-453A>T XP_016867980.1:n.280-453A>T
NM_002889.4:c.280-453A>T MANE Select NP_002880.1:n.280-453A>T