Canonical Allele Identifier: CA35752035
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs76834242
MyVariant Identifiers: chr1:g.204190231C>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204190231C>G , CM000663.2:g.204190231C>G GRCh38
NC_000001.10:g.204159359C>G , CM000663.1:g.204159359C>G GRCh37
NC_000001.9:g.202425982C>G NCBI36
NG_032151.1:g.11261G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000638118.1:c.-211+1G>C ENSP00000490307.1:n.-211+1G>C