Canonical Allele Identifier: CA344338221
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204128635A>T (hg19) chr1:g.204159507A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159507A>T , CM000663.2:g.204159507A>T GRCh38
NC_000001.10:g.204128635A>T , CM000663.1:g.204128635A>T GRCh37
NC_000001.9:g.202395258A>T NCBI36
NG_012122.1:g.11831T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.581T>A MANE Select ENSP00000272190.8:p.Val194Glu
ENST00000638118.1:c.467T>A ENSP00000490307.1:p.Val156Glu
ENST00000272190.8:c.581T>A ENSP00000272190.8:p.Val194Glu
NM_000537.3:c.581T>A NP_000528.1:p.Val194Glu
NM_000537.4:c.581T>A MANE Select NP_000528.1:p.Val194Glu
Search 100 bp 5'
Search 100 bp 3'