Canonical Allele Identifier: CA2013876614

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6031410C= , CM000674.2:g.6031410C=	GRCh38
NC_000012.11:g.6140576C= , CM000674.1:g.6140576C=	GRCh37
NC_000012.10:g.6010837C=	NCBI36
NG_009072.1:g.98261G=
NG_009072.2:g.98261G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261405.10:c.2820+34G= MANE Select	ENSP00000261405.5:n.2820+34G=
ENST00000261405.9:c.2820+34G=	ENSP00000261405.5:n.2820+34G=
ENST00000538635.5:n.421-37476G=
NM_000552.3:c.2820+34G=	NP_000543.2:n.2820+34G=
NM_000552.4:c.2820+34G=	NP_000543.2:n.2820+34G=
NM_000552.5:c.2820+34G= MANE Select	NP_000543.3:n.2820+34G=