Canonical Allele Identifier: CA422837365
Gene: REN HGNC NCBI

Linked Data

gnomAD v4: 1-204159461-G-A
COSMIC: COSM6459942
MyVariant Identifiers: chr1:g.204128589G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159461G>A , CM000663.2:g.204159461G>A GRCh38
NC_000001.10:g.204128589G>A , CM000663.1:g.204128589G>A GRCh37
NC_000001.9:g.202395212G>A NCBI36
NG_012122.1:g.11877C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.627C>T MANE Select ENSP00000272190.8:p.Ile209=
ENST00000638118.1:c.513C>T ENSP00000490307.1:p.Ile171=
ENST00000272190.8:c.627C>T ENSP00000272190.8:p.Ile209=
NM_000537.3:c.627C>T NP_000528.1:p.Ile209=
NM_000537.4:c.627C>T MANE Select NP_000528.1:p.Ile209=
Search 100 bp 5'
Search 100 bp 3'