Canonical Allele Identifier: CA1011400033
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs1658201087

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159267A>G , CM000663.2:g.204159267A>G GRCh38
NC_000001.10:g.204128395A>G , CM000663.1:g.204128395A>G GRCh37
NC_000001.9:g.202395018A>G NCBI36
NG_012122.1:g.12071T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.689+132T>C MANE Select ENSP00000272190.8:n.689+132T>C
ENST00000638118.1:c.575+132T>C ENSP00000490307.1:n.575+132T>C
ENST00000272190.8:c.689+132T>C ENSP00000272190.8:n.689+132T>C
NM_000537.3:c.689+132T>C NP_000528.1:n.689+132T>C
NM_000537.4:c.689+132T>C MANE Select NP_000528.1:n.689+132T>C