Canonical Allele Identifier: CA1790512049

Linked Data

dbSNP Id: rs1807321153

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.66469015A>G , CM000670.2:g.66469015A>G GRCh38
NC_000008.10:g.67381250A>G , CM000670.1:g.67381250A>G GRCh37
NC_000008.9:g.67543804A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000648156.1:c.*540-2415A>G ENSP00000497007.1:n.*540-2415A>G
ENST00000480040.5:n.396-2415A>G (ADHFE1)
ENST00000482608.6:n.250+8550A>G (VXN)
ENST00000519702.5:n.162+8550A>G (VXN)