Canonical Allele Identifier: CA344338609
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs985476332
MyVariant Identifiers: chr1:g.204128692C>T (hg19) chr1:g.204159564C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159564C>T , CM000663.2:g.204159564C>T GRCh38
NC_000001.10:g.204128692C>T , CM000663.1:g.204128692C>T GRCh37
NC_000001.9:g.202395315C>T NCBI36
NG_012122.1:g.11774G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.524G>A MANE Select ENSP00000272190.8:p.Gly175Glu
ENST00000638118.1:c.410G>A ENSP00000490307.1:p.Gly137Glu
ENST00000272190.8:c.524G>A ENSP00000272190.8:p.Gly175Glu
NM_000537.3:c.524G>A NP_000528.1:p.Gly175Glu
NM_000537.4:c.524G>A MANE Select NP_000528.1:p.Gly175Glu
Search 100 bp 5'
Search 100 bp 3'