Canonical Allele Identifier: CA2013880780

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6036143C= , CM000674.2:g.6036143C=	GRCh38
NC_000012.11:g.6145309C= , CM000674.1:g.6145309C=	GRCh37
NC_000012.10:g.6015570C=	NCBI36
NG_009072.1:g.93528G=
NG_009072.2:g.93528G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.2546+245G= MANE Select	ENSP00000261405.5:n.2546+245G=
ENST00000261405.9:c.2546+245G=	ENSP00000261405.5:n.2546+245G=
ENST00000538635.5:n.421-42209G=
NM_000552.3:c.2546+245G=	NP_000543.2:n.2546+245G=
NM_000552.4:c.2546+245G=	NP_000543.2:n.2546+245G=
NM_000552.5:c.2546+245G= MANE Select	NP_000543.3:n.2546+245G=