Canonical Allele Identifier: CA2617233710

Gene: VWF

Linked Data

• gnomAD v4: 12-6072464-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6072467dup , CM000674.2:g.6072467dup	GRCh38
NC_000012.11:g.6181633dup , CM000674.1:g.6181633dup	GRCh37
NC_000012.10:g.6051894dup	NCBI36
NG_009072.1:g.57206dup
NG_009072.2:g.57206dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.998-23dup MANE Select	ENSP00000261405.5:n.998-23dup
ENST00000261405.9:c.998-23dup	ENSP00000261405.5:n.998-23dup
ENST00000538635.5:n.420+38050dup
NM_000552.3:c.998-23dup	NP_000543.2:n.998-23dup
NM_000552.4:c.998-23dup	NP_000543.2:n.998-23dup
NM_000552.5:c.998-23dup MANE Select	NP_000543.3:n.998-23dup