Canonical Allele Identifier: CA35739656
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs962454810
gnomAD v3: 1-204165444-G-T
gnomAD v4: 1-204165444-G-T
MyVariant Identifiers: chr1:g.204134572G>T (hg19) chr1:g.204165444G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204165444G>T , CM000663.2:g.204165444G>T GRCh38
NC_000001.10:g.204134572G>T , CM000663.1:g.204134572G>T GRCh37
NC_000001.9:g.202401195G>T NCBI36
NG_012122.1:g.5894C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000272190.9:c.98+752C>A MANE Select ENSP00000272190.8:n.98+752C>A
ENST00000638118.1:c.-16-3281C>A ENSP00000490307.1:n.-16-3281C>A
ENST00000272190.8:c.98+752C>A ENSP00000272190.8:n.98+752C>A
NM_000537.3:c.98+752C>A NP_000528.1:n.98+752C>A
NM_000537.4:c.98+752C>A MANE Select NP_000528.1:n.98+752C>A
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