Canonical Allele Identifier: CA2013875057

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6023893T= , CM000674.2:g.6023893T=	GRCh38
NC_000012.11:g.6133059T= , CM000674.1:g.6133059T=	GRCh37
NC_000012.10:g.6003320T=	NCBI36
NG_009072.1:g.105778A=
NG_009072.2:g.105778A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.3223-106A= MANE Select	ENSP00000261405.5:n.3223-106A=
ENST00000261405.9:c.3223-106A=	ENSP00000261405.5:n.3223-106A=
ENST00000538635.5:n.421-29959A=
NM_000552.3:c.3223-106A=	NP_000543.2:n.3223-106A=
NM_000552.4:c.3223-106A=	NP_000543.2:n.3223-106A=
NM_000552.5:c.3223-106A= MANE Select	NP_000543.3:n.3223-106A=