Canonical Allele Identifier: CA1790512069

Linked Data

dbSNP Id: rs1807322408

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.66469064G>A , CM000670.2:g.66469064G>A GRCh38
NC_000008.10:g.67381299G>A , CM000670.1:g.67381299G>A GRCh37
NC_000008.9:g.67543853G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000648156.1:c.*540-2366G>A ENSP00000497007.1:n.*540-2366G>A
ENST00000480040.5:n.396-2366G>A (ADHFE1)
ENST00000482608.6:n.250+8599G>A (VXN)
ENST00000519702.5:n.162+8599G>A (VXN)