Canonical Allele Identifier: CA730343268
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs1241026685
MyVariant Identifiers: chr1:g.204134462A>T (hg19) chr1:g.204165334A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204165334A>T , CM000663.2:g.204165334A>T GRCh38
NC_000001.10:g.204134462A>T , CM000663.1:g.204134462A>T GRCh37
NC_000001.9:g.202401085A>T NCBI36
NG_012122.1:g.6004T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000272190.9:c.98+862T>A MANE Select ENSP00000272190.8:n.98+862T>A
ENST00000638118.1:c.-16-3171T>A ENSP00000490307.1:n.-16-3171T>A
ENST00000272190.8:c.98+862T>A ENSP00000272190.8:n.98+862T>A
NM_000537.3:c.98+862T>A NP_000528.1:n.98+862T>A
NM_000537.4:c.98+862T>A MANE Select NP_000528.1:n.98+862T>A
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