Canonical Allele Identifier: CA2013849799
Gene: VWF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5969006T= , CM000674.2:g.5969006T= GRCh38
NC_000012.11:g.6078172T= , CM000674.1:g.6078172T= GRCh37
NC_000012.10:g.5948433T= NCBI36
NG_009072.1:g.160665A=
NG_009072.2:g.160665A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.7729+205A= MANE Select ENSP00000261405.5:n.7729+205A=
ENST00000261405.9:c.7729+205A= ENSP00000261405.5:n.7729+205A=
NM_000552.3:c.7729+205A= NP_000543.2:n.7729+205A=
NM_000552.4:c.7729+205A= NP_000543.2:n.7729+205A=
NM_000552.5:c.7729+205A= MANE Select NP_000543.3:n.7729+205A=