Canonical Allele Identifier: CA422837383
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204128603T>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159475T>G , CM000663.2:g.204159475T>G GRCh38
NC_000001.10:g.204128603T>G , CM000663.1:g.204128603T>G GRCh37
NC_000001.9:g.202395226T>G NCBI36
NG_012122.1:g.11863A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.613A>C MANE Select ENSP00000272190.8:p.Arg205=
ENST00000638118.1:c.499A>C ENSP00000490307.1:p.Arg167=
ENST00000272190.8:c.613A>C ENSP00000272190.8:p.Arg205=
NM_000537.3:c.613A>C NP_000528.1:p.Arg205=
NM_000537.4:c.613A>C MANE Select NP_000528.1:p.Arg205=
Search 100 bp 5'
Search 100 bp 3'