Canonical Allele Identifier: CA422837322
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204128541A>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159413A>C , CM000663.2:g.204159413A>C GRCh38
NC_000001.10:g.204128541A>C , CM000663.1:g.204128541A>C GRCh37
NC_000001.9:g.202395164A>C NCBI36
NG_012122.1:g.11925T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.675T>G MANE Select ENSP00000272190.8:p.Ser225=
ENST00000638118.1:c.561T>G ENSP00000490307.1:p.Ser187=
ENST00000272190.8:c.675T>G ENSP00000272190.8:p.Ser225=
NM_000537.3:c.675T>G NP_000528.1:p.Ser225=
NM_000537.4:c.675T>G MANE Select NP_000528.1:p.Ser225=
Search 100 bp 5'
Search 100 bp 3'