Canonical Allele Identifier: CA344338484
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204128668A>G (hg19) chr1:g.204159540A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159540A>G , CM000663.2:g.204159540A>G GRCh38
NC_000001.10:g.204128668A>G , CM000663.1:g.204128668A>G GRCh37
NC_000001.9:g.202395291A>G NCBI36
NG_012122.1:g.11798T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.548T>C MANE Select ENSP00000272190.8:p.Leu183Ser
ENST00000638118.1:c.434T>C ENSP00000490307.1:p.Leu145Ser
ENST00000272190.8:c.548T>C ENSP00000272190.8:p.Leu183Ser
NM_000537.3:c.548T>C NP_000528.1:p.Leu183Ser
NM_000537.4:c.548T>C MANE Select NP_000528.1:p.Leu183Ser
Search 100 bp 5'
Search 100 bp 3'