Canonical Allele Identifier: CA422837380
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204128601C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159473C>T , CM000663.2:g.204159473C>T GRCh38
NC_000001.10:g.204128601C>T , CM000663.1:g.204128601C>T GRCh37
NC_000001.9:g.202395224C>T NCBI36
NG_012122.1:g.11865G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.615G>A MANE Select ENSP00000272190.8:p.Arg205=
ENST00000638118.1:c.501G>A ENSP00000490307.1:p.Arg167=
ENST00000272190.8:c.615G>A ENSP00000272190.8:p.Arg205=
NM_000537.3:c.615G>A NP_000528.1:p.Arg205=
NM_000537.4:c.615G>A MANE Select NP_000528.1:p.Arg205=
Search 100 bp 5'
Search 100 bp 3'