Canonical Allele Identifier: CA2013874076

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6021900C= , CM000674.2:g.6021900C=	GRCh38
NC_000012.11:g.6131066C= , CM000674.1:g.6131066C=	GRCh37
NC_000012.10:g.6001327C=	NCBI36
NG_009072.1:g.107771G=
NG_009072.2:g.107771G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261405.10:c.3674G= MANE Select	ENSP00000261405.5:p.Cys1225=
ENST00000261405.9:c.3674G=	ENSP00000261405.5:p.Cys1225=
ENST00000538635.5:n.421-27966G=
ENST00000539641.1:n.27G=
NM_000552.3:c.3674G=	NP_000543.2:p.Cys1225=
NM_000552.4:c.3674G=	NP_000543.2:p.Cys1225=
NM_000552.5:c.3674G= MANE Select	NP_000543.3:p.Cys1225=