Canonical Allele Identifier: CA178472066

Linked Data

dbSNP Id: rs934928819

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.66469048T>G , CM000670.2:g.66469048T>G GRCh38
NC_000008.10:g.67381283T>G , CM000670.1:g.67381283T>G GRCh37
NC_000008.9:g.67543837T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000648156.1:c.*540-2382T>G ENSP00000497007.1:n.*540-2382T>G
ENST00000480040.5:n.396-2382T>G (ADHFE1)
ENST00000482608.6:n.250+8583T>G (VXN)
ENST00000519702.5:n.162+8583T>G (VXN)