Canonical Allele Identifier: CA2013874184

Gene: VWF

Linked Data

• dbSNP Id: rs1944136570

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6022154G>T , CM000674.2:g.6022154G>T	GRCh38
NC_000012.11:g.6131320G>T , CM000674.1:g.6131320G>T	GRCh37
NC_000012.10:g.6001581G>T	NCBI36
NG_009072.1:g.107517C>A
NG_009072.2:g.107517C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.3539-119C>A MANE Select	ENSP00000261405.5:n.3539-119C>A
ENST00000261405.9:c.3539-119C>A	ENSP00000261405.5:n.3539-119C>A
ENST00000538635.5:n.421-28220C>A
NM_000552.3:c.3539-119C>A	NP_000543.2:n.3539-119C>A
NM_000552.4:c.3539-119C>A	NP_000543.2:n.3539-119C>A
NM_000552.5:c.3539-119C>A MANE Select	NP_000543.3:n.3539-119C>A