Canonical Allele Identifier: CA1772915370

Genomic Alleles

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

Transcript Alleles

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