Canonical Allele Identifier: CA2697918959
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs2102312659

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159326G>A , CM000663.2:g.204159326G>A GRCh38
NC_000001.10:g.204128454G>A , CM000663.1:g.204128454G>A GRCh37
NC_000001.9:g.202395077G>A NCBI36
NG_012122.1:g.12012C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.689+73C>T MANE Select ENSP00000272190.8:n.689+73C>T
ENST00000638118.1:c.575+73C>T ENSP00000490307.1:n.575+73C>T
ENST00000272190.8:c.689+73C>T ENSP00000272190.8:n.689+73C>T
NM_000537.3:c.689+73C>T NP_000528.1:n.689+73C>T
NM_000537.4:c.689+73C>T MANE Select NP_000528.1:n.689+73C>T