Canonical Allele Identifier: CA228447
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100282
ClinVar RCV Id: RCV000086680
dbSNP Id: rs61749372

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6019604A>C , CM000674.2:g.6019604A>C GRCh38
NC_000012.11:g.6128770A>C , CM000674.1:g.6128770A>C GRCh37
NC_000012.10:g.5999031A>C NCBI36
NG_009072.1:g.110067T>G
NG_009072.2:g.110067T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261405.10:c.3814T>G MANE Select ENSP00000261405.5:p.Cys1272Gly
ENST00000261405.9:c.3814T>G ENSP00000261405.5:p.Cys1272Gly
ENST00000538635.5:n.421-25670T>G
ENST00000539641.1:n.612T>G
NM_000552.3:c.3814T>G NP_000543.2:p.Cys1272Gly
NM_000552.4:c.3814T>G NP_000543.2:p.Cys1272Gly
NM_000552.5:c.3814T>G MANE Select NP_000543.3:p.Cys1272Gly