Canonical Allele Identifier: CA2013873017
Gene: VWF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6019504T= , CM000674.2:g.6019504T= GRCh38
NC_000012.11:g.6128670T= , CM000674.1:g.6128670T= GRCh37
NC_000012.10:g.5998931T= NCBI36
NG_009072.1:g.110167A=
NG_009072.2:g.110167A=

Transcript Alleles

HGVS Amino-acid change
ENST00000261405.10:c.3914A= MANE Select ENSP00000261405.5:p.Glu1305=
ENST00000261405.9:c.3914A= ENSP00000261405.5:p.Glu1305=
ENST00000538635.5:n.421-25570A=
NM_000552.3:c.3914A= NP_000543.2:p.Glu1305=
NM_000552.4:c.3914A= NP_000543.2:p.Glu1305=
NM_000552.5:c.3914A= MANE Select NP_000543.3:p.Glu1305=