Canonical Allele Identifier: CA422837397
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204128616T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159488T>C , CM000663.2:g.204159488T>C GRCh38
NC_000001.10:g.204128616T>C , CM000663.1:g.204128616T>C GRCh37
NC_000001.9:g.202395239T>C NCBI36
NG_012122.1:g.11850A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.600A>G MANE Select ENSP00000272190.8:p.Glu200=
ENST00000638118.1:c.486A>G ENSP00000490307.1:p.Glu162=
ENST00000272190.8:c.600A>G ENSP00000272190.8:p.Glu200=
NM_000537.3:c.600A>G NP_000528.1:p.Glu200=
NM_000537.4:c.600A>G MANE Select NP_000528.1:p.Glu200=
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Search 100 bp 3'