Canonical Allele Identifier: CA2013872489

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6018385G= , CM000674.2:g.6018385G=	GRCh38
NC_000012.11:g.6127551G= , CM000674.1:g.6127551G=	GRCh37
NC_000012.10:g.5997812G=	NCBI36
NG_009072.1:g.111286C=
NG_009072.2:g.111286C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.5033C= MANE Select	ENSP00000261405.5:p.Pro1678=
ENST00000261405.9:c.5033C=	ENSP00000261405.5:p.Pro1678=
ENST00000538635.5:n.421-24451C=
NM_000552.3:c.5033C=	NP_000543.2:p.Pro1678=
NM_000552.4:c.5033C=	NP_000543.2:p.Pro1678=
NM_000552.5:c.5033C= MANE Select	NP_000543.3:p.Pro1678=