Canonical Allele Identifier: CA344337945
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204128587A>T (hg19) chr1:g.204159459A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159459A>T , CM000663.2:g.204159459A>T GRCh38
NC_000001.10:g.204128587A>T , CM000663.1:g.204128587A>T GRCh37
NC_000001.9:g.202395210A>T NCBI36
NG_012122.1:g.11879T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.629T>A MANE Select ENSP00000272190.8:p.Phe210Tyr
ENST00000638118.1:c.515T>A ENSP00000490307.1:p.Phe172Tyr
ENST00000272190.8:c.629T>A ENSP00000272190.8:p.Phe210Tyr
NM_000537.3:c.629T>A NP_000528.1:p.Phe210Tyr
NM_000537.4:c.629T>A MANE Select NP_000528.1:p.Phe210Tyr
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