Canonical Allele Identifier: CA2013874819
Gene: VWF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6023556A= , CM000674.2:g.6023556A= GRCh38
NC_000012.11:g.6132722A= , CM000674.1:g.6132722A= GRCh37
NC_000012.10:g.6002983A= NCBI36
NG_009072.1:g.106115T=
NG_009072.2:g.106115T=

Transcript Alleles

HGVS Amino-acid change
ENST00000261405.10:c.3379+75T= MANE Select ENSP00000261405.5:n.3379+75T=
ENST00000261405.9:c.3379+75T= ENSP00000261405.5:n.3379+75T=
ENST00000538635.5:n.421-29622T=
NM_000552.3:c.3379+75T= NP_000543.2:n.3379+75T=
NM_000552.4:c.3379+75T= NP_000543.2:n.3379+75T=
NM_000552.5:c.3379+75T= MANE Select NP_000543.3:n.3379+75T=