Canonical Allele Identifier: CA344337622
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204128539A>T (hg19) chr1:g.204159411A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159411A>T , CM000663.2:g.204159411A>T GRCh38
NC_000001.10:g.204128539A>T , CM000663.1:g.204128539A>T GRCh37
NC_000001.9:g.202395162A>T NCBI36
NG_012122.1:g.11927T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000272190.9:c.677T>A MANE Select ENSP00000272190.8:p.Phe226Tyr
ENST00000638118.1:c.563T>A ENSP00000490307.1:p.Phe188Tyr
ENST00000272190.8:c.677T>A ENSP00000272190.8:p.Phe226Tyr
NM_000537.3:c.677T>A NP_000528.1:p.Phe226Tyr
NM_000537.4:c.677T>A MANE Select NP_000528.1:p.Phe226Tyr
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