Canonical Allele Identifier: CA344338005
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs1558244577

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159473C>A , CM000663.2:g.204159473C>A GRCh38
NC_000001.10:g.204128601C>A , CM000663.1:g.204128601C>A GRCh37
NC_000001.9:g.202395224C>A NCBI36
NG_012122.1:g.11865G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.615G>T MANE Select ENSP00000272190.8:p.Arg205Ser
ENST00000638118.1:c.501G>T ENSP00000490307.1:p.Arg167Ser
ENST00000272190.8:c.615G>T ENSP00000272190.8:p.Arg205Ser
NM_000537.3:c.615G>T NP_000528.1:p.Arg205Ser
NM_000537.4:c.615G>T MANE Select NP_000528.1:p.Arg205Ser