Canonical Allele Identifier: CA2013892450

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6058190G= , CM000674.2:g.6058190G=	GRCh38
NC_000012.11:g.6167356G= , CM000674.1:g.6167356G=	GRCh37
NC_000012.10:g.6037617G=	NCBI36
NG_009072.1:g.71481C=
NG_009072.2:g.71481C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.1534-146C= MANE Select	ENSP00000261405.5:n.1534-146C=
ENST00000261405.9:c.1534-146C=	ENSP00000261405.5:n.1534-146C=
ENST00000538635.5:n.420+52325C=
NM_000552.3:c.1534-146C=	NP_000543.2:n.1534-146C=
NM_000552.4:c.1534-146C=	NP_000543.2:n.1534-146C=
NM_000552.5:c.1534-146C= MANE Select	NP_000543.3:n.1534-146C=