Canonical Allele Identifier: CA344338188
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs1658206212

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159501A>G , CM000663.2:g.204159501A>G GRCh38
NC_000001.10:g.204128629A>G , CM000663.1:g.204128629A>G GRCh37
NC_000001.9:g.202395252A>G NCBI36
NG_012122.1:g.11837T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.587T>C MANE Select ENSP00000272190.8:p.Met196Thr
ENST00000638118.1:c.473T>C ENSP00000490307.1:p.Met158Thr
ENST00000272190.8:c.587T>C ENSP00000272190.8:p.Met196Thr
NM_000537.3:c.587T>C NP_000528.1:p.Met196Thr
NM_000537.4:c.587T>C MANE Select NP_000528.1:p.Met196Thr