Canonical Allele Identifier: CA1772920525
Community Standard Title: NC_000008.11:g.27584547G=

Genomic Alleles

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

Transcript Alleles

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