Canonical Allele Identifier: CA2013876871

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6031647A= , CM000674.2:g.6031647A=	GRCh38
NC_000012.11:g.6140813A= , CM000674.1:g.6140813A=	GRCh37
NC_000012.10:g.6011074A=	NCBI36
NG_009072.1:g.98024T=
NG_009072.2:g.98024T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.2686-69T= MANE Select	ENSP00000261405.5:n.2686-69T=
ENST00000261405.9:c.2686-69T=	ENSP00000261405.5:n.2686-69T=
ENST00000538635.5:n.421-37713T=
NM_000552.3:c.2686-69T=	NP_000543.2:n.2686-69T=
NM_000552.4:c.2686-69T=	NP_000543.2:n.2686-69T=
NM_000552.5:c.2686-69T= MANE Select	NP_000543.3:n.2686-69T=