Canonical Allele Identifier: CA2013874712

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6023307T= , CM000674.2:g.6023307T=	GRCh38
NC_000012.11:g.6132473T= , CM000674.1:g.6132473T=	GRCh37
NC_000012.10:g.6002734T=	NCBI36
NG_009072.1:g.106364A=
NG_009072.2:g.106364A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.3379+324A= MANE Select	ENSP00000261405.5:n.3379+324A=
ENST00000261405.9:c.3379+324A=	ENSP00000261405.5:n.3379+324A=
ENST00000538635.5:n.421-29373A=
NM_000552.3:c.3379+324A=	NP_000543.2:n.3379+324A=
NM_000552.4:c.3379+324A=	NP_000543.2:n.3379+324A=
NM_000552.5:c.3379+324A= MANE Select	NP_000543.3:n.3379+324A=