Canonical Allele Identifier: CA528191371
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs1366460357
gnomAD v2: 1-204134487-T-A
gnomAD v3: 1-204165359-T-A
gnomAD v4: 1-204165359-T-A
MyVariant Identifiers: chr1:g.204134487T>A (hg19) chr1:g.204165359T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204165359T>A , CM000663.2:g.204165359T>A GRCh38
NC_000001.10:g.204134487T>A , CM000663.1:g.204134487T>A GRCh37
NC_000001.9:g.202401110T>A NCBI36
NG_012122.1:g.5979A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000272190.9:c.98+837A>T MANE Select ENSP00000272190.8:n.98+837A>T
ENST00000638118.1:c.-16-3196A>T ENSP00000490307.1:n.-16-3196A>T
ENST00000272190.8:c.98+837A>T ENSP00000272190.8:n.98+837A>T
NM_000537.3:c.98+837A>T NP_000528.1:n.98+837A>T
NM_000537.4:c.98+837A>T MANE Select NP_000528.1:n.98+837A>T
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