Canonical Allele Identifier: CA2013874911
Gene: VWF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6023740G= , CM000674.2:g.6023740G= GRCh38
NC_000012.11:g.6132906G= , CM000674.1:g.6132906G= GRCh37
NC_000012.10:g.6003167G= NCBI36
NG_009072.1:g.105931C=
NG_009072.2:g.105931C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.3270C= MANE Select ENSP00000261405.5:p.Ser1090=
ENST00000261405.9:c.3270C= ENSP00000261405.5:p.Ser1090=
ENST00000538635.5:n.421-29806C=
NM_000552.3:c.3270C= NP_000543.2:p.Ser1090=
NM_000552.4:c.3270C= NP_000543.2:p.Ser1090=
NM_000552.5:c.3270C= MANE Select NP_000543.3:p.Ser1090=