Canonical Allele Identifier: CA1999654392

Linked Data

dbSNP Id: rs4561177

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.110091706A>C , CM000673.2:g.110091706A>C GRCh38
NC_000011.9:g.109962432A>C , CM000673.1:g.109962432A>C GRCh37
NC_000011.8:g.109467642A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645527.1:c.*757+32353T>G (RDX) ENSP00000496121.1:n.*757+32353T>G
XM_011543056.1:c.-73+3105A>C (ZC3H12C) XP_011541358.1:n.-73+3105A>C