Canonical Allele Identifier: CA2013874785

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6023474A= , CM000674.2:g.6023474A=	GRCh38
NC_000012.11:g.6132640A= , CM000674.1:g.6132640A=	GRCh37
NC_000012.10:g.6002901A=	NCBI36
NG_009072.1:g.106197T=
NG_009072.2:g.106197T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.3379+157T= MANE Select	ENSP00000261405.5:n.3379+157T=
ENST00000261405.9:c.3379+157T=	ENSP00000261405.5:n.3379+157T=
ENST00000538635.5:n.421-29540T=
NM_000552.3:c.3379+157T=	NP_000543.2:n.3379+157T=
NM_000552.4:c.3379+157T=	NP_000543.2:n.3379+157T=
NM_000552.5:c.3379+157T= MANE Select	NP_000543.3:n.3379+157T=