Canonical Allele Identifier: CA344338259
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204128641C>G (hg19) chr1:g.204159513C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159513C>G , CM000663.2:g.204159513C>G GRCh38
NC_000001.10:g.204128641C>G , CM000663.1:g.204128641C>G GRCh37
NC_000001.9:g.202395264C>G NCBI36
NG_012122.1:g.11825G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.575G>C MANE Select ENSP00000272190.8:p.Gly192Ala
ENST00000638118.1:c.461G>C ENSP00000490307.1:p.Gly154Ala
ENST00000272190.8:c.575G>C ENSP00000272190.8:p.Gly192Ala
NM_000537.3:c.575G>C NP_000528.1:p.Gly192Ala
NM_000537.4:c.575G>C MANE Select NP_000528.1:p.Gly192Ala
Search 100 bp 5'
Search 100 bp 3'