Canonical Allele Identifier: CA10948558
Gene: REN HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11240688

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204165394G>A , CM000663.2:g.204165394G>A GRCh38
NC_000001.10:g.204134522G>A , CM000663.1:g.204134522G>A GRCh37
NC_000001.9:g.202401145G>A NCBI36
NG_012122.1:g.5944C>T

Transcript Alleles

HGVS Amino-acid change
NM_000537.3:c.98+802C>T VV NP_000528.1:p.=
NM_000537.4:c.98+802C>T VV MANE Preferred NP_000528.1:p.=
ENST00000272190.8:c.98+802C>T ENSP00000272190.8:p.=