Canonical Allele Identifier: CA2013897882

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6072439C= , CM000674.2:g.6072439C=	GRCh38
NC_000012.11:g.6181605C= , CM000674.1:g.6181605C=	GRCh37
NC_000012.10:g.6051866C=	NCBI36
NG_009072.1:g.57232G=
NG_009072.2:g.57232G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.1001G= MANE Select	ENSP00000261405.5:p.Gly334=
ENST00000261405.9:c.1001G=	ENSP00000261405.5:p.Gly334=
ENST00000538635.5:n.420+38076G=
NM_000552.3:c.1001G=	NP_000543.2:p.Gly334=
NM_000552.4:c.1001G=	NP_000543.2:p.Gly334=
NM_000552.5:c.1001G= MANE Select	NP_000543.3:p.Gly334=