Canonical Allele Identifier: CA2013880882
Gene: VWF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6036345C= , CM000674.2:g.6036345C= GRCh38
NC_000012.11:g.6145511C= , CM000674.1:g.6145511C= GRCh37
NC_000012.10:g.6015772C= NCBI36
NG_009072.1:g.93326G=
NG_009072.2:g.93326G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.2546+43G= MANE Select ENSP00000261405.5:n.2546+43G=
ENST00000261405.9:c.2546+43G= ENSP00000261405.5:n.2546+43G=
ENST00000538635.5:n.421-42411G=
NM_000552.3:c.2546+43G= NP_000543.2:n.2546+43G=
NM_000552.4:c.2546+43G= NP_000543.2:n.2546+43G=
NM_000552.5:c.2546+43G= MANE Select NP_000543.3:n.2546+43G=
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