Canonical Allele Identifier: CA1345022
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs778600672

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204162026G>C , CM000663.2:g.204162026G>C GRCh38
NC_000001.10:g.204131154G>C , CM000663.1:g.204131154G>C GRCh37
NC_000001.9:g.202397777G>C NCBI36
NG_012122.1:g.9312C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.236C>G MANE Select ENSP00000272190.8:p.Thr79Ser
ENST00000638118.1:c.122C>G ENSP00000490307.1:p.Thr41Ser
ENST00000272190.8:c.236C>G ENSP00000272190.8:p.Thr79Ser
NM_000537.3:c.236C>G NP_000528.1:p.Thr79Ser
NM_000537.4:c.236C>G MANE Select NP_000528.1:p.Thr79Ser