Canonical Allele Identifier: CA422837392
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204128610G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159482G>C , CM000663.2:g.204159482G>C GRCh38
NC_000001.10:g.204128610G>C , CM000663.1:g.204128610G>C GRCh37
NC_000001.9:g.202395233G>C NCBI36
NG_012122.1:g.11856C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.606C>G MANE Select ENSP00000272190.8:p.Ala202=
ENST00000638118.1:c.492C>G ENSP00000490307.1:p.Ala164=
ENST00000272190.8:c.606C>G ENSP00000272190.8:p.Ala202=
NM_000537.3:c.606C>G NP_000528.1:p.Ala202=
NM_000537.4:c.606C>G MANE Select NP_000528.1:p.Ala202=
Search 100 bp 5'
Search 100 bp 3'