Canonical Allele Identifier: CA2482055301
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs1248453322

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204155205T>A , CM000663.2:g.204155205T>A GRCh38
NC_000001.10:g.204124333T>A , CM000663.1:g.204124333T>A GRCh37
NC_000001.9:g.202390956T>A NCBI36
NG_012122.1:g.16133A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.1060-28A>T MANE Select ENSP00000272190.8:n.1060-28A>T
ENST00000638118.1:c.946-28A>T ENSP00000490307.1:n.946-28A>T
ENST00000272190.8:c.1060-28A>T ENSP00000272190.8:n.1060-28A>T
NM_000537.3:c.1060-28A>T NP_000528.1:n.1060-28A>T
NM_000537.4:c.1060-28A>T MANE Select NP_000528.1:n.1060-28A>T