Canonical Allele Identifier: CA344338368
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204128656A>C (hg19) chr1:g.204159528A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159528A>C , CM000663.2:g.204159528A>C GRCh38
NC_000001.10:g.204128656A>C , CM000663.1:g.204128656A>C GRCh37
NC_000001.9:g.202395279A>C NCBI36
NG_012122.1:g.11810T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.560T>G MANE Select ENSP00000272190.8:p.Leu187Arg
ENST00000638118.1:c.446T>G ENSP00000490307.1:p.Leu149Arg
ENST00000272190.8:c.560T>G ENSP00000272190.8:p.Leu187Arg
NM_000537.3:c.560T>G NP_000528.1:p.Leu187Arg
NM_000537.4:c.560T>G MANE Select NP_000528.1:p.Leu187Arg
Search 100 bp 5'
Search 100 bp 3'