Canonical Allele Identifier: CA730338842
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs1164566540
MyVariant Identifiers: chr1:g.204128440A>G (hg19) chr1:g.204159312A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159312A>G , CM000663.2:g.204159312A>G GRCh38
NC_000001.10:g.204128440A>G , CM000663.1:g.204128440A>G GRCh37
NC_000001.9:g.202395063A>G NCBI36
NG_012122.1:g.12026T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000272190.9:c.689+87T>C MANE Select ENSP00000272190.8:n.689+87T>C
ENST00000638118.1:c.575+87T>C ENSP00000490307.1:n.575+87T>C
ENST00000272190.8:c.689+87T>C ENSP00000272190.8:n.689+87T>C
NM_000537.3:c.689+87T>C NP_000528.1:n.689+87T>C
NM_000537.4:c.689+87T>C MANE Select NP_000528.1:n.689+87T>C
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