Canonical Allele Identifier: CA2013875018

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6023852T= , CM000674.2:g.6023852T=	GRCh38
NC_000012.11:g.6133018T= , CM000674.1:g.6133018T=	GRCh37
NC_000012.10:g.6003279T=	NCBI36
NG_009072.1:g.105819A=
NG_009072.2:g.105819A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.3223-65A= MANE Select	ENSP00000261405.5:n.3223-65A=
ENST00000261405.9:c.3223-65A=	ENSP00000261405.5:n.3223-65A=
ENST00000538635.5:n.421-29918A=
NM_000552.3:c.3223-65A=	NP_000543.2:n.3223-65A=
NM_000552.4:c.3223-65A=	NP_000543.2:n.3223-65A=
NM_000552.5:c.3223-65A= MANE Select	NP_000543.3:n.3223-65A=