Canonical Allele Identifier: CA1344885
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs778838428
ExAC: 1:204128632 C / T
gnomAD v2: 1-204128632-C-T
gnomAD v4: 1-204159504-C-T
MyVariant Identifiers: chr1:g.204128632C>T (hg19) chr1:g.204159504C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159504C>T , CM000663.2:g.204159504C>T GRCh38
NC_000001.10:g.204128632C>T , CM000663.1:g.204128632C>T GRCh37
NC_000001.9:g.202395255C>T NCBI36
NG_012122.1:g.11834G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.584G>A MANE Select ENSP00000272190.8:p.Gly195Asp
ENST00000638118.1:c.470G>A ENSP00000490307.1:p.Gly157Asp
ENST00000272190.8:c.584G>A ENSP00000272190.8:p.Gly195Asp
NM_000537.3:c.584G>A NP_000528.1:p.Gly195Asp
NM_000537.4:c.584G>A MANE Select NP_000528.1:p.Gly195Asp
Search 100 bp 5'
Search 100 bp 3'