Canonical Allele Identifier: CA422839368
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204131254G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204162126G>A , CM000663.2:g.204162126G>A GRCh38
NC_000001.10:g.204131254G>A , CM000663.1:g.204131254G>A GRCh37
NC_000001.9:g.202397877G>A NCBI36
NG_012122.1:g.9212C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000272190.9:c.136C>T MANE Select ENSP00000272190.8:p.Leu46=
ENST00000638118.1:c.22C>T ENSP00000490307.1:p.Leu8=
ENST00000272190.8:c.136C>T ENSP00000272190.8:p.Leu46=
NM_000537.3:c.136C>T NP_000528.1:p.Leu46=
NM_000537.4:c.136C>T MANE Select NP_000528.1:p.Leu46=
Search 100 bp 5'
Search 100 bp 3'