Canonical Allele Identifier: CA2575054138

Gene: VWF

Linked Data

• gnomAD v4: 12-6036358-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6036362dup , CM000674.2:g.6036362dup	GRCh38
NC_000012.11:g.6145528dup , CM000674.1:g.6145528dup	GRCh37
NC_000012.10:g.6015789dup	NCBI36
NG_009072.1:g.93312dup
NG_009072.2:g.93312dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.2546+29dup MANE Select	ENSP00000261405.5:n.2546+29dup
ENST00000261405.9:c.2546+29dup	ENSP00000261405.5:n.2546+29dup
ENST00000538635.5:n.421-42425dup
NM_000552.3:c.2546+29dup	NP_000543.2:n.2546+29dup
NM_000552.4:c.2546+29dup	NP_000543.2:n.2546+29dup
NM_000552.5:c.2546+29dup MANE Select	NP_000543.3:n.2546+29dup