Canonical Allele Identifier: CA1790512032

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.66468976G= , CM000670.2:g.66468976G= GRCh38
NC_000008.10:g.67381211G= , CM000670.1:g.67381211G= GRCh37
NC_000008.9:g.67543765G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000648156.1:c.*540-2454G= ENSP00000497007.1:n.*540-2454G=
ENST00000480040.5:n.396-2454G= (ADHFE1)
ENST00000482608.6:n.250+8511G= (VXN)
ENST00000519702.5:n.162+8511G= (VXN)