Canonical Allele Identifier: CA2013875097

Gene: VWF

Linked Data

• dbSNP Id: rs1944162603

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6023932_6023933del , CM000674.2:g.6023932_6023933del	GRCh38
NC_000012.11:g.6133098_6133099del , CM000674.1:g.6133098_6133099del	GRCh37
NC_000012.10:g.6003359_6003360del	NCBI36
NG_009072.1:g.105740_105741del
NG_009072.2:g.105740_105741del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.3223-144_3223-143del MANE Select	ENSP00000261405.5:n.3223-144_3223-143del
ENST00000261405.9:c.3223-144_3223-143del	ENSP00000261405.5:n.3223-144_3223-143del
ENST00000538635.5:n.421-29997_421-29996del
NM_000552.3:c.3223-144_3223-143del	NP_000543.2:n.3223-144_3223-143del
NM_000552.4:c.3223-144_3223-143del	NP_000543.2:n.3223-144_3223-143del
NM_000552.5:c.3223-144_3223-143del MANE Select	NP_000543.3:n.3223-144_3223-143del