Canonical Allele Identifier: CA344337928
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204128583G>C (hg19) chr1:g.204159455G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159455G>C , CM000663.2:g.204159455G>C GRCh38
NC_000001.10:g.204128583G>C , CM000663.1:g.204128583G>C GRCh37
NC_000001.9:g.202395206G>C NCBI36
NG_012122.1:g.11883C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.633C>G MANE Select ENSP00000272190.8:p.Asp211Glu
ENST00000638118.1:c.519C>G ENSP00000490307.1:p.Asp173Glu
ENST00000272190.8:c.633C>G ENSP00000272190.8:p.Asp211Glu
NM_000537.3:c.633C>G NP_000528.1:p.Asp211Glu
NM_000537.4:c.633C>G MANE Select NP_000528.1:p.Asp211Glu
Search 100 bp 5'
Search 100 bp 3'