Canonical Allele Identifier: CA2013897898

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6072474A= , CM000674.2:g.6072474A=	GRCh38
NC_000012.11:g.6181640A= , CM000674.1:g.6181640A=	GRCh37
NC_000012.10:g.6051901A=	NCBI36
NG_009072.1:g.57197T=
NG_009072.2:g.57197T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.998-32T= MANE Select	ENSP00000261405.5:n.998-32T=
ENST00000261405.9:c.998-32T=	ENSP00000261405.5:n.998-32T=
ENST00000538635.5:n.420+38041T=
NM_000552.3:c.998-32T=	NP_000543.2:n.998-32T=
NM_000552.4:c.998-32T=	NP_000543.2:n.998-32T=
NM_000552.5:c.998-32T= MANE Select	NP_000543.3:n.998-32T=