Canonical Allele Identifier: CA12787290

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.27572989A>G , CM000670.2:g.27572989A>G GRCh38
NC_000008.10:g.27430506A>G , CM000670.1:g.27430506A>G GRCh37
NC_000008.9:g.27486423A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000454030.1:n.198-4622A>G (GULOP)
XR_001745491.1:n.1648-19344A>G (EPHX2)