Canonical Allele Identifier: CA2013892410

Gene: VWF

Linked Data

• dbSNP Id: rs1944611306

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6058147del , CM000674.2:g.6058147del	GRCh38
NC_000012.11:g.6167313del , CM000674.1:g.6167313del	GRCh37
NC_000012.10:g.6037574del	NCBI36
NG_009072.1:g.71526del
NG_009072.2:g.71526del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.1534-101del MANE Select	ENSP00000261405.5:n.1534-101del
ENST00000261405.9:c.1534-101del	ENSP00000261405.5:n.1534-101del
ENST00000538635.5:n.420+52370del
NM_000552.3:c.1534-101del	NP_000543.2:n.1534-101del
NM_000552.4:c.1534-101del	NP_000543.2:n.1534-101del
NM_000552.5:c.1534-101del MANE Select	NP_000543.3:n.1534-101del