Canonical Allele Identifier: CA2013849792
Gene: VWF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5968994C= , CM000674.2:g.5968994C= GRCh38
NC_000012.11:g.6078160C= , CM000674.1:g.6078160C= GRCh37
NC_000012.10:g.5948421C= NCBI36
NG_009072.1:g.160677G=
NG_009072.2:g.160677G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.7729+217G= MANE Select ENSP00000261405.5:n.7729+217G=
ENST00000261405.9:c.7729+217G= ENSP00000261405.5:n.7729+217G=
NM_000552.3:c.7729+217G= NP_000543.2:n.7729+217G=
NM_000552.4:c.7729+217G= NP_000543.2:n.7729+217G=
NM_000552.5:c.7729+217G= MANE Select NP_000543.3:n.7729+217G=
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