Canonical Allele Identifier: CA344338033
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204128606C>T (hg19) chr1:g.204159478C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159478C>T , CM000663.2:g.204159478C>T GRCh38
NC_000001.10:g.204128606C>T , CM000663.1:g.204128606C>T GRCh37
NC_000001.9:g.202395229C>T NCBI36
NG_012122.1:g.11860G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.610G>A MANE Select ENSP00000272190.8:p.Gly204Ser
ENST00000638118.1:c.496G>A ENSP00000490307.1:p.Gly166Ser
ENST00000272190.8:c.610G>A ENSP00000272190.8:p.Gly204Ser
NM_000537.3:c.610G>A NP_000528.1:p.Gly204Ser
NM_000537.4:c.610G>A MANE Select NP_000528.1:p.Gly204Ser
Search 100 bp 5'
Search 100 bp 3'