Canonical Allele Identifier: CA228498
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100308
ClinVar RCV Id: RCV000086710
dbSNP Id: rs61749393

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6019478C>A , CM000674.2:g.6019478C>A GRCh38
NC_000012.11:g.6128644C>A , CM000674.1:g.6128644C>A GRCh37
NC_000012.10:g.5998905C>A NCBI36
NG_009072.1:g.110193G>T
NG_009072.2:g.110193G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.3940G>T MANE Select ENSP00000261405.5:p.Val1314Phe
ENST00000261405.9:c.3940G>T ENSP00000261405.5:p.Val1314Phe
ENST00000538635.5:n.421-25544G>T
NM_000552.3:c.3940G>T NP_000543.2:p.Val1314Phe
NM_000552.4:c.3940G>T NP_000543.2:p.Val1314Phe
NM_000552.5:c.3940G>T MANE Select NP_000543.3:p.Val1314Phe