Canonical Allele Identifier: CA344337990
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204128597T>G (hg19) chr1:g.204159469T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159469T>G , CM000663.2:g.204159469T>G GRCh38
NC_000001.10:g.204128597T>G , CM000663.1:g.204128597T>G GRCh37
NC_000001.9:g.202395220T>G NCBI36
NG_012122.1:g.11869A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.619A>C MANE Select ENSP00000272190.8:p.Thr207Pro
ENST00000638118.1:c.505A>C ENSP00000490307.1:p.Thr169Pro
ENST00000272190.8:c.619A>C ENSP00000272190.8:p.Thr207Pro
NM_000537.3:c.619A>C NP_000528.1:p.Thr207Pro
NM_000537.4:c.619A>C MANE Select NP_000528.1:p.Thr207Pro
Search 100 bp 5'
Search 100 bp 3'