Canonical Allele Identifier: CA422840577
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204135385G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204166257G>A , CM000663.2:g.204166257G>A GRCh38
NC_000001.10:g.204135385G>A , CM000663.1:g.204135385G>A GRCh37
NC_000001.9:g.202402008G>A NCBI36
NG_012122.1:g.5081C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000272190.9:c.37C>T MANE Select ENSP00000272190.8:p.Leu13=
ENST00000638118.1:c.-16-4094C>T ENSP00000490307.1:n.-16-4094C>T
ENST00000272190.8:c.37C>T ENSP00000272190.8:p.Leu13=
NM_000537.3:c.37C>T NP_000528.1:p.Leu13=
NM_000537.4:c.37C>T MANE Select NP_000528.1:p.Leu13=
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Search 100 bp 3'