Canonical Allele Identifier: CA2013874907
Gene: VWF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6023735T= , CM000674.2:g.6023735T= GRCh38
NC_000012.11:g.6132901T= , CM000674.1:g.6132901T= GRCh37
NC_000012.10:g.6003162T= NCBI36
NG_009072.1:g.105936A=
NG_009072.2:g.105936A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.3275A= MANE Select ENSP00000261405.5:p.Glu1092=
ENST00000261405.9:c.3275A= ENSP00000261405.5:p.Glu1092=
ENST00000538635.5:n.421-29801A=
NM_000552.3:c.3275A= NP_000543.2:p.Glu1092=
NM_000552.4:c.3275A= NP_000543.2:p.Glu1092=
NM_000552.5:c.3275A= MANE Select NP_000543.3:p.Glu1092=