Canonical Allele Identifier: CA35739491
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs372755503
MyVariant Identifiers: chr1:g.204134365T>C (hg19) chr1:g.204165237T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204165237T>C , CM000663.2:g.204165237T>C GRCh38
NC_000001.10:g.204134365T>C , CM000663.1:g.204134365T>C GRCh37
NC_000001.9:g.202400988T>C NCBI36
NG_012122.1:g.6101A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000272190.9:c.98+959A>G MANE Select ENSP00000272190.8:n.98+959A>G
ENST00000638118.1:c.-16-3074A>G ENSP00000490307.1:n.-16-3074A>G
ENST00000272190.8:c.98+959A>G ENSP00000272190.8:n.98+959A>G
NM_000537.3:c.98+959A>G NP_000528.1:n.98+959A>G
NM_000537.4:c.98+959A>G MANE Select NP_000528.1:n.98+959A>G
Search 100 bp 5'
Search 100 bp 3'