Canonical Allele Identifier: CA2013880742

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6036045T= , CM000674.2:g.6036045T=	GRCh38
NC_000012.11:g.6145211T= , CM000674.1:g.6145211T=	GRCh37
NC_000012.10:g.6015472T=	NCBI36
NG_009072.1:g.93626A=
NG_009072.2:g.93626A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.2546+343A= MANE Select	ENSP00000261405.5:n.2546+343A=
ENST00000261405.9:c.2546+343A=	ENSP00000261405.5:n.2546+343A=
ENST00000538635.5:n.421-42111A=
NM_000552.3:c.2546+343A=	NP_000543.2:n.2546+343A=
NM_000552.4:c.2546+343A=	NP_000543.2:n.2546+343A=
NM_000552.5:c.2546+343A= MANE Select	NP_000543.3:n.2546+343A=