Canonical Allele Identifier: CA2013874915
Gene: VWF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6023746G= , CM000674.2:g.6023746G= GRCh38
NC_000012.11:g.6132912G= , CM000674.1:g.6132912G= GRCh37
NC_000012.10:g.6003173G= NCBI36
NG_009072.1:g.105925C=
NG_009072.2:g.105925C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.3264C= MANE Select ENSP00000261405.5:p.Thr1088=
ENST00000261405.9:c.3264C= ENSP00000261405.5:p.Thr1088=
ENST00000538635.5:n.421-29812C=
NM_000552.3:c.3264C= NP_000543.2:p.Thr1088=
NM_000552.4:c.3264C= NP_000543.2:p.Thr1088=
NM_000552.5:c.3264C= MANE Select NP_000543.3:p.Thr1088=