Canonical Allele Identifier: CA2013872530
Gene: VWF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6018474A= , CM000674.2:g.6018474A= GRCh38
NC_000012.11:g.6127640A= , CM000674.1:g.6127640A= GRCh37
NC_000012.10:g.5997901A= NCBI36
NG_009072.1:g.111197T=
NG_009072.2:g.111197T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.4944T= MANE Select ENSP00000261405.5:p.Pro1648=
ENST00000261405.9:c.4944T= ENSP00000261405.5:p.Pro1648=
ENST00000538635.5:n.421-24540T=
NM_000552.3:c.4944T= NP_000543.2:p.Pro1648=
NM_000552.4:c.4944T= NP_000543.2:p.Pro1648=
NM_000552.5:c.4944T= MANE Select NP_000543.3:p.Pro1648=