Canonical Allele Identifier: CA919013153

Gene: VWF

Linked Data

• dbSNP Id: rs1565836718

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6031643del , CM000674.2:g.6031643del	GRCh38
NC_000012.11:g.6140809del , CM000674.1:g.6140809del	GRCh37
NC_000012.10:g.6011070del	NCBI36
NG_009072.1:g.98029del
NG_009072.2:g.98029del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.2686-64del MANE Select	ENSP00000261405.5:n.2686-64del
ENST00000261405.9:c.2686-64del	ENSP00000261405.5:n.2686-64del
ENST00000538635.5:n.421-37708del
NM_000552.3:c.2686-64del	NP_000543.2:n.2686-64del
NM_000552.4:c.2686-64del	NP_000543.2:n.2686-64del
NM_000552.5:c.2686-64del MANE Select	NP_000543.3:n.2686-64del