Canonical Allele Identifier: CA2013873012

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6019496G= , CM000674.2:g.6019496G=	GRCh38
NC_000012.11:g.6128662G= , CM000674.1:g.6128662G=	GRCh37
NC_000012.10:g.5998923G=	NCBI36
NG_009072.1:g.110175C=
NG_009072.2:g.110175C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261405.10:c.3922C= MANE Select	ENSP00000261405.5:p.Arg1308=
ENST00000261405.9:c.3922C=	ENSP00000261405.5:p.Arg1308=
ENST00000538635.5:n.421-25562C=
NM_000552.3:c.3922C=	NP_000543.2:p.Arg1308=
NM_000552.4:c.3922C=	NP_000543.2:p.Arg1308=
NM_000552.5:c.3922C= MANE Select	NP_000543.3:p.Arg1308=