Canonical Allele Identifier: CA12720006

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.27584547G>A , CM000670.2:g.27584547G>A GRCh38
NC_000008.10:g.27442064G>A , CM000670.1:g.27442064G>A GRCh37
NC_000008.9:g.27497981G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000454030.1:n.305-1413G>A (GULOP)
XR_001745491.1:n.1648-7786G>A (EPHX2)