Canonical Allele Identifier: CA6402722
Gene: VWF HGNC NCBI

Linked Data

dbSNP Id: rs768331524
gnomAD v2: 12-6131118-A-G
gnomAD v4: 12-6021952-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6021952A>G , CM000674.2:g.6021952A>G GRCh38
NC_000012.11:g.6131118A>G , CM000674.1:g.6131118A>G GRCh37
NC_000012.10:g.6001379A>G NCBI36
NG_009072.1:g.107719T>C
NG_009072.2:g.107719T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.3622T>C MANE Select ENSP00000261405.5:p.Ser1208Pro
ENST00000261405.9:c.3622T>C ENSP00000261405.5:p.Ser1208Pro
ENST00000538635.5:n.421-28018T>C
NM_000552.3:c.3622T>C NP_000543.2:p.Ser1208Pro
NM_000552.4:c.3622T>C NP_000543.2:p.Ser1208Pro
NM_000552.5:c.3622T>C MANE Select NP_000543.3:p.Ser1208Pro