Canonical Allele Identifier: CA2013873016

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6019502G= , CM000674.2:g.6019502G=	GRCh38
NC_000012.11:g.6128668G= , CM000674.1:g.6128668G=	GRCh37
NC_000012.10:g.5998929G=	NCBI36
NG_009072.1:g.110169C=
NG_009072.2:g.110169C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261405.10:c.3916C= MANE Select	ENSP00000261405.5:p.Arg1306=
ENST00000261405.9:c.3916C=	ENSP00000261405.5:p.Arg1306=
ENST00000538635.5:n.421-25568C=
NM_000552.3:c.3916C=	NP_000543.2:p.Arg1306=
NM_000552.4:c.3916C=	NP_000543.2:p.Arg1306=
NM_000552.5:c.3916C= MANE Select	NP_000543.3:p.Arg1306=