Canonical Allele Identifier: CA2013876619

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6031413G= , CM000674.2:g.6031413G=	GRCh38
NC_000012.11:g.6140579G= , CM000674.1:g.6140579G=	GRCh37
NC_000012.10:g.6010840G=	NCBI36
NG_009072.1:g.98258C=
NG_009072.2:g.98258C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261405.10:c.2820+31C= MANE Select	ENSP00000261405.5:n.2820+31C=
ENST00000261405.9:c.2820+31C=	ENSP00000261405.5:n.2820+31C=
ENST00000538635.5:n.421-37479C=
NM_000552.3:c.2820+31C=	NP_000543.2:n.2820+31C=
NM_000552.4:c.2820+31C=	NP_000543.2:n.2820+31C=
NM_000552.5:c.2820+31C= MANE Select	NP_000543.3:n.2820+31C=