Canonical Allele Identifier: CA2013876714

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6031499T= , CM000674.2:g.6031499T=	GRCh38
NC_000012.11:g.6140665T= , CM000674.1:g.6140665T=	GRCh37
NC_000012.10:g.6010926T=	NCBI36
NG_009072.1:g.98172A=
NG_009072.2:g.98172A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.2765A= MANE Select	ENSP00000261405.5:p.Lys922=
ENST00000261405.9:c.2765A=	ENSP00000261405.5:p.Lys922=
ENST00000538635.5:n.421-37565A=
NM_000552.3:c.2765A=	NP_000543.2:p.Lys922=
NM_000552.4:c.2765A=	NP_000543.2:p.Lys922=
NM_000552.5:c.2765A= MANE Select	NP_000543.3:p.Lys922=