Canonical Allele Identifier: CA913375975
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs1558246656
gnomAD v2: 1-204134461-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204165333C>A , CM000663.2:g.204165333C>A GRCh38
NC_000001.10:g.204134461C>A , CM000663.1:g.204134461C>A GRCh37
NC_000001.9:g.202401084C>A NCBI36
NG_012122.1:g.6005G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.98+863G>T MANE Select ENSP00000272190.8:n.98+863G>T
ENST00000638118.1:c.-16-3170G>T ENSP00000490307.1:n.-16-3170G>T
ENST00000272190.8:c.98+863G>T ENSP00000272190.8:n.98+863G>T
NM_000537.3:c.98+863G>T NP_000528.1:n.98+863G>T
NM_000537.4:c.98+863G>T MANE Select NP_000528.1:n.98+863G>T
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