Canonical Allele Identifier: CA422837411
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204128625G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159497G>A , CM000663.2:g.204159497G>A GRCh38
NC_000001.10:g.204128625G>A , CM000663.1:g.204128625G>A GRCh37
NC_000001.9:g.202395248G>A NCBI36
NG_012122.1:g.11841C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.591C>T MANE Select ENSP00000272190.8:p.Gly197=
ENST00000638118.1:c.477C>T ENSP00000490307.1:p.Gly159=
ENST00000272190.8:c.591C>T ENSP00000272190.8:p.Gly197=
NM_000537.3:c.591C>T NP_000528.1:p.Gly197=
NM_000537.4:c.591C>T MANE Select NP_000528.1:p.Gly197=