Canonical Allele Identifier: CA2013880172

Gene: VWF

Linked Data

• dbSNP Id: rs1944316986

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6034832A>G , CM000674.2:g.6034832A>G	GRCh38
NC_000012.11:g.6143998A>G , CM000674.1:g.6143998A>G	GRCh37
NC_000012.10:g.6014259A>G	NCBI36
NG_009072.1:g.94839T>C
NG_009072.2:g.94839T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261405.10:c.2547-6T>C MANE Select	ENSP00000261405.5:n.2547-6T>C
ENST00000261405.9:c.2547-6T>C	ENSP00000261405.5:n.2547-6T>C
ENST00000538635.5:n.421-40898T>C
NM_000552.3:c.2547-6T>C	NP_000543.2:n.2547-6T>C
NM_000552.4:c.2547-6T>C	NP_000543.2:n.2547-6T>C
NM_000552.5:c.2547-6T>C MANE Select	NP_000543.3:n.2547-6T>C