Canonical Allele Identifier: CA2794406783

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6058082C>T , CM000674.2:g.6058082C>T	GRCh38
NC_000012.11:g.6167248C>T , CM000674.1:g.6167248C>T	GRCh37
NC_000012.10:g.6037509C>T	NCBI36
NG_009072.1:g.71589G>A
NG_009072.2:g.71589G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.1534-38G>A MANE Select	ENSP00000261405.5:n.1534-38G>A
ENST00000261405.9:c.1534-38G>A	ENSP00000261405.5:n.1534-38G>A
ENST00000538635.5:n.420+52433G>A
NM_000552.3:c.1534-38G>A	NP_000543.2:n.1534-38G>A
NM_000552.4:c.1534-38G>A	NP_000543.2:n.1534-38G>A
NM_000552.5:c.1534-38G>A MANE Select	NP_000543.3:n.1534-38G>A