Canonical Allele Identifier: CA1790512019

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.66468948A= , CM000670.2:g.66468948A= GRCh38
NC_000008.10:g.67381183A= , CM000670.1:g.67381183A= GRCh37
NC_000008.9:g.67543737A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000648156.1:c.*540-2482A= ENSP00000497007.1:n.*540-2482A=
ENST00000480040.5:n.396-2482A= (ADHFE1)
ENST00000482608.6:n.250+8483A= (VXN)
ENST00000519702.5:n.162+8483A= (VXN)