Canonical Allele Identifier: CA422837460
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204128691T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159563T>G , CM000663.2:g.204159563T>G GRCh38
NC_000001.10:g.204128691T>G , CM000663.1:g.204128691T>G GRCh37
NC_000001.9:g.202395314T>G NCBI36
NG_012122.1:g.11775A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.525A>C MANE Select ENSP00000272190.8:p.Gly175=
ENST00000638118.1:c.411A>C ENSP00000490307.1:p.Gly137=
ENST00000272190.8:c.525A>C ENSP00000272190.8:p.Gly175=
NM_000537.3:c.525A>C NP_000528.1:p.Gly175=
NM_000537.4:c.525A>C MANE Select NP_000528.1:p.Gly175=