Canonical Allele Identifier: CA2013872487

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6018383T= , CM000674.2:g.6018383T=	GRCh38
NC_000012.11:g.6127549T= , CM000674.1:g.6127549T=	GRCh37
NC_000012.10:g.5997810T=	NCBI36
NG_009072.1:g.111288A=
NG_009072.2:g.111288A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.5035A= MANE Select	ENSP00000261405.5:p.Thr1679=
ENST00000261405.9:c.5035A=	ENSP00000261405.5:p.Thr1679=
ENST00000538635.5:n.421-24449A=
NM_000552.3:c.5035A=	NP_000543.2:p.Thr1679=
NM_000552.4:c.5035A=	NP_000543.2:p.Thr1679=
NM_000552.5:c.5035A= MANE Select	NP_000543.3:p.Thr1679=