Canonical Allele Identifier: CA344338048
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204128609T>A (hg19) chr1:g.204159481T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159481T>A , CM000663.2:g.204159481T>A GRCh38
NC_000001.10:g.204128609T>A , CM000663.1:g.204128609T>A GRCh37
NC_000001.9:g.202395232T>A NCBI36
NG_012122.1:g.11857A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.607A>T MANE Select ENSP00000272190.8:p.Ile203Phe
ENST00000638118.1:c.493A>T ENSP00000490307.1:p.Ile165Phe
ENST00000272190.8:c.607A>T ENSP00000272190.8:p.Ile203Phe
NM_000537.3:c.607A>T NP_000528.1:p.Ile203Phe
NM_000537.4:c.607A>T MANE Select NP_000528.1:p.Ile203Phe
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