Canonical Allele Identifier: CA2013871529
Gene: VWF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6016246A= , CM000674.2:g.6016246A= GRCh38
NC_000012.11:g.6125412A= , CM000674.1:g.6125412A= GRCh37
NC_000012.10:g.5995673A= NCBI36
NG_009072.1:g.113425T=
NG_009072.2:g.113425T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.5312-14T= MANE Select ENSP00000261405.5:n.5312-14T=
ENST00000261405.9:c.5312-14T= ENSP00000261405.5:n.5312-14T=
ENST00000538635.5:n.421-22312T=
NM_000552.3:c.5312-14T= NP_000543.2:n.5312-14T=
NM_000552.4:c.5312-14T= NP_000543.2:n.5312-14T=
NM_000552.5:c.5312-14T= MANE Select NP_000543.3:n.5312-14T=