Canonical Allele Identifier: CA2013876962
Gene: VWF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6031754G= , CM000674.2:g.6031754G= GRCh38
NC_000012.11:g.6140920G= , CM000674.1:g.6140920G= GRCh37
NC_000012.10:g.6011181G= NCBI36
NG_009072.1:g.97917C=
NG_009072.2:g.97917C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.2686-176C= MANE Select ENSP00000261405.5:n.2686-176C=
ENST00000261405.9:c.2686-176C= ENSP00000261405.5:n.2686-176C=
ENST00000538635.5:n.421-37820C=
NM_000552.3:c.2686-176C= NP_000543.2:n.2686-176C=
NM_000552.4:c.2686-176C= NP_000543.2:n.2686-176C=
NM_000552.5:c.2686-176C= MANE Select NP_000543.3:n.2686-176C=
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