Canonical Allele Identifier: CA2013874115

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6022008G= , CM000674.2:g.6022008G=	GRCh38
NC_000012.11:g.6131174G= , CM000674.1:g.6131174G=	GRCh37
NC_000012.10:g.6001435G=	NCBI36
NG_009072.1:g.107663C=
NG_009072.2:g.107663C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261405.10:c.3566C= MANE Select	ENSP00000261405.5:p.Thr1189=
ENST00000261405.9:c.3566C=	ENSP00000261405.5:p.Thr1189=
ENST00000538635.5:n.421-28074C=
NM_000552.3:c.3566C=	NP_000543.2:p.Thr1189=
NM_000552.4:c.3566C=	NP_000543.2:p.Thr1189=
NM_000552.5:c.3566C= MANE Select	NP_000543.3:p.Thr1189=