Canonical Allele Identifier: CA6403087
Gene: VWF HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 256660
dbSNP Id: rs1063857

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6044348A>G , CM000674.2:g.6044348A>G GRCh38
NC_000012.11:g.6153514A>G , CM000674.1:g.6153514A>G GRCh37
NC_000012.10:g.6023775A>G NCBI36
NG_009072.1:g.85323T>C

Transcript Alleles

HGVS Amino-acid change
NM_000552.3:c.2385T>C VV NP_000543.2:p.Tyr795=
NM_000552.4:c.2385T>C VV
ENST00000261405.9:c.2385T>C ENSP00000261405.5:p.Tyr795=
ENST00000538635.5:n.421-50414T>C