Canonical Allele Identifier: CA1011400583
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs1422151114

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204160554A>C , CM000663.2:g.204160554A>C GRCh38
NC_000001.10:g.204129682A>C , CM000663.1:g.204129682A>C GRCh37
NC_000001.9:g.202396305A>C NCBI36
NG_012122.1:g.10784T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.492+6T>G MANE Select ENSP00000272190.8:n.492+6T>G
ENST00000638118.1:c.378+6T>G ENSP00000490307.1:n.378+6T>G
ENST00000272190.8:c.492+6T>G ENSP00000272190.8:n.492+6T>G
NM_000537.3:c.492+6T>G NP_000528.1:n.492+6T>G
NM_000537.4:c.492+6T>G MANE Select NP_000528.1:n.492+6T>G