Canonical Allele Identifier: CA1790512051

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.66469022T= , CM000670.2:g.66469022T= GRCh38
NC_000008.10:g.67381257T= , CM000670.1:g.67381257T= GRCh37
NC_000008.9:g.67543811T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000648156.1:c.*540-2408T= ENSP00000497007.1:n.*540-2408T=
ENST00000480040.5:n.396-2408T= (ADHFE1)
ENST00000482608.6:n.250+8557T= (VXN)
ENST00000519702.5:n.162+8557T= (VXN)