Canonical Allele Identifier: CA1345023
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs574100052

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204162032A>G , CM000663.2:g.204162032A>G GRCh38
NC_000001.10:g.204131160A>G , CM000663.1:g.204131160A>G GRCh37
NC_000001.9:g.202397783A>G NCBI36
NG_012122.1:g.9306T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.230T>C MANE Select ENSP00000272190.8:p.Ile77Thr
ENST00000638118.1:c.116T>C ENSP00000490307.1:p.Ile39Thr
ENST00000272190.8:c.230T>C ENSP00000272190.8:p.Ile77Thr
NM_000537.3:c.230T>C NP_000528.1:p.Ile77Thr
NM_000537.4:c.230T>C MANE Select NP_000528.1:p.Ile77Thr