Canonical Allele Identifier: CA2013849778
Gene: VWF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5968959T= , CM000674.2:g.5968959T= GRCh38
NC_000012.11:g.6078125T= , CM000674.1:g.6078125T= GRCh37
NC_000012.10:g.5948386T= NCBI36
NG_009072.1:g.160712A=
NG_009072.2:g.160712A=

Transcript Alleles

HGVS Amino-acid change
ENST00000261405.10:c.7729+252A= MANE Select ENSP00000261405.5:n.7729+252A=
ENST00000261405.9:c.7729+252A= ENSP00000261405.5:n.7729+252A=
NM_000552.3:c.7729+252A= NP_000543.2:n.7729+252A=
NM_000552.4:c.7729+252A= NP_000543.2:n.7729+252A=
NM_000552.5:c.7729+252A= MANE Select NP_000543.3:n.7729+252A=
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