Canonical Allele Identifier: CA2013849779
Gene: VWF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5968965G= , CM000674.2:g.5968965G= GRCh38
NC_000012.11:g.6078131G= , CM000674.1:g.6078131G= GRCh37
NC_000012.10:g.5948392G= NCBI36
NG_009072.1:g.160706C=
NG_009072.2:g.160706C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.7729+246C= MANE Select ENSP00000261405.5:n.7729+246C=
ENST00000261405.9:c.7729+246C= ENSP00000261405.5:n.7729+246C=
NM_000552.3:c.7729+246C= NP_000543.2:n.7729+246C=
NM_000552.4:c.7729+246C= NP_000543.2:n.7729+246C=
NM_000552.5:c.7729+246C= MANE Select NP_000543.3:n.7729+246C=
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