Canonical Allele Identifier: CA344332267
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204124207G>C (hg19) chr1:g.204155079G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204155079G>C , CM000663.2:g.204155079G>C GRCh38
NC_000001.10:g.204124207G>C , CM000663.1:g.204124207G>C GRCh37
NC_000001.9:g.202390830G>C NCBI36
NG_012122.1:g.16259C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000272190.9:c.1158C>G MANE Select ENSP00000272190.8:p.Ile386Met
ENST00000638118.1:c.1044C>G ENSP00000490307.1:p.Ile348Met
ENST00000272190.8:c.1158C>G ENSP00000272190.8:p.Ile386Met
NM_000537.3:c.1158C>G NP_000528.1:p.Ile386Met
NM_000537.4:c.1158C>G MANE Select NP_000528.1:p.Ile386Met
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