Canonical Allele Identifier: CA344338334
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204128651C>G (hg19) chr1:g.204159523C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159523C>G , CM000663.2:g.204159523C>G GRCh38
NC_000001.10:g.204128651C>G , CM000663.1:g.204128651C>G GRCh37
NC_000001.9:g.202395274C>G NCBI36
NG_012122.1:g.11815G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.565G>C MANE Select ENSP00000272190.8:p.Glu189Gln
ENST00000638118.1:c.451G>C ENSP00000490307.1:p.Glu151Gln
ENST00000272190.8:c.565G>C ENSP00000272190.8:p.Glu189Gln
NM_000537.3:c.565G>C NP_000528.1:p.Glu189Gln
NM_000537.4:c.565G>C MANE Select NP_000528.1:p.Glu189Gln
Search 100 bp 5'
Search 100 bp 3'