Canonical Allele Identifier: CA422833169
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204124219C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204155091C>T , CM000663.2:g.204155091C>T GRCh38
NC_000001.10:g.204124219C>T , CM000663.1:g.204124219C>T GRCh37
NC_000001.9:g.202390842C>T NCBI36
NG_012122.1:g.16247G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000272190.9:c.1146G>A MANE Select ENSP00000272190.8:p.Gly382=
ENST00000638118.1:c.1032G>A ENSP00000490307.1:p.Gly344=
ENST00000272190.8:c.1146G>A ENSP00000272190.8:p.Gly382=
NM_000537.3:c.1146G>A NP_000528.1:p.Gly382=
NM_000537.4:c.1146G>A MANE Select NP_000528.1:p.Gly382=
Search 100 bp 5'
Search 100 bp 3'