Canonical Allele Identifier: CA2013880171
Gene: VWF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6034832A= , CM000674.2:g.6034832A= GRCh38
NC_000012.11:g.6143998A= , CM000674.1:g.6143998A= GRCh37
NC_000012.10:g.6014259A= NCBI36
NG_009072.1:g.94839T=
NG_009072.2:g.94839T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.2547-6T= MANE Select ENSP00000261405.5:n.2547-6T=
ENST00000261405.9:c.2547-6T= ENSP00000261405.5:n.2547-6T=
ENST00000538635.5:n.421-40898T=
NM_000552.3:c.2547-6T= NP_000543.2:n.2547-6T=
NM_000552.4:c.2547-6T= NP_000543.2:n.2547-6T=
NM_000552.5:c.2547-6T= MANE Select NP_000543.3:n.2547-6T=