Canonical Allele Identifier: CA178472060

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.66469033G>A , CM000670.2:g.66469033G>A GRCh38
NC_000008.10:g.67381268G>A , CM000670.1:g.67381268G>A GRCh37
NC_000008.9:g.67543822G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000648156.1:c.*540-2397G>A ENSP00000497007.1:n.*540-2397G>A
ENST00000480040.5:n.396-2397G>A (ADHFE1)
ENST00000482608.6:n.250+8568G>A (VXN)
ENST00000519702.5:n.162+8568G>A (VXN)