Canonical Allele Identifier: CA2013871455

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6016095A= , CM000674.2:g.6016095A=	GRCh38
NC_000012.11:g.6125261A= , CM000674.1:g.6125261A=	GRCh37
NC_000012.10:g.5995522A=	NCBI36
NG_009072.1:g.113576T=
NG_009072.2:g.113576T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.5449T= MANE Select	ENSP00000261405.5:p.Ser1817=
ENST00000261405.9:c.5449T=	ENSP00000261405.5:p.Ser1817=
ENST00000538635.5:n.421-22161T=
NM_000552.3:c.5449T=	NP_000543.2:p.Ser1817=
NM_000552.4:c.5449T=	NP_000543.2:p.Ser1817=
NM_000552.5:c.5449T= MANE Select	NP_000543.3:p.Ser1817=