Canonical Allele Identifier: CA2695215972
Gene: VWF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6058043_6058045del , CM000674.2:g.6058043_6058045del GRCh38
NC_000012.11:g.6167209_6167211del , CM000674.1:g.6167209_6167211del GRCh37
NC_000012.10:g.6037470_6037472del NCBI36
NG_009072.1:g.71627_71629del
NG_009072.2:g.71627_71629del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.1534_1536del
ENST00000261405.9:c.1534_1536del
ENST00000538635.5:n.420+52471_420+52473del
NM_000552.3:c.1534_1536del
NM_000552.4:c.1534_1536del
NM_000552.5:c.1534_1536del