Canonical Allele Identifier: CA2013892361

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6058112G= , CM000674.2:g.6058112G=	GRCh38
NC_000012.11:g.6167278G= , CM000674.1:g.6167278G=	GRCh37
NC_000012.10:g.6037539G=	NCBI36
NG_009072.1:g.71559C=
NG_009072.2:g.71559C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.1534-68C= MANE Select	ENSP00000261405.5:n.1534-68C=
ENST00000261405.9:c.1534-68C=	ENSP00000261405.5:n.1534-68C=
ENST00000538635.5:n.420+52403C=
NM_000552.3:c.1534-68C=	NP_000543.2:n.1534-68C=
NM_000552.4:c.1534-68C=	NP_000543.2:n.1534-68C=
NM_000552.5:c.1534-68C= MANE Select	NP_000543.3:n.1534-68C=