Canonical Allele Identifier: CA2013880787

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6036153C= , CM000674.2:g.6036153C=	GRCh38
NC_000012.11:g.6145319C= , CM000674.1:g.6145319C=	GRCh37
NC_000012.10:g.6015580C=	NCBI36
NG_009072.1:g.93518G=
NG_009072.2:g.93518G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.2546+235G= MANE Select	ENSP00000261405.5:n.2546+235G=
ENST00000261405.9:c.2546+235G=	ENSP00000261405.5:n.2546+235G=
ENST00000538635.5:n.421-42219G=
NM_000552.3:c.2546+235G=	NP_000543.2:n.2546+235G=
NM_000552.4:c.2546+235G=	NP_000543.2:n.2546+235G=
NM_000552.5:c.2546+235G= MANE Select	NP_000543.3:n.2546+235G=