Canonical Allele Identifier: CA422837374
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204128595G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159467G>T , CM000663.2:g.204159467G>T GRCh38
NC_000001.10:g.204128595G>T , CM000663.1:g.204128595G>T GRCh37
NC_000001.9:g.202395218G>T NCBI36
NG_012122.1:g.11871C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.621C>A MANE Select ENSP00000272190.8:p.Thr207=
ENST00000638118.1:c.507C>A ENSP00000490307.1:p.Thr169=
ENST00000272190.8:c.621C>A ENSP00000272190.8:p.Thr207=
NM_000537.3:c.621C>A NP_000528.1:p.Thr207=
NM_000537.4:c.621C>A MANE Select NP_000528.1:p.Thr207=
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