Canonical Allele Identifier: CA2013874236

Gene: VWF

Linked Data

• dbSNP Id: rs1591865206

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6022261A>C , CM000674.2:g.6022261A>C	GRCh38
NC_000012.11:g.6131427A>C , CM000674.1:g.6131427A>C	GRCh37
NC_000012.10:g.6001688A>C	NCBI36
NG_009072.1:g.107410T>G
NG_009072.2:g.107410T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.3539-226T>G MANE Select	ENSP00000261405.5:n.3539-226T>G
ENST00000261405.9:c.3539-226T>G	ENSP00000261405.5:n.3539-226T>G
ENST00000538635.5:n.421-28327T>G
NM_000552.3:c.3539-226T>G	NP_000543.2:n.3539-226T>G
NM_000552.4:c.3539-226T>G	NP_000543.2:n.3539-226T>G
NM_000552.5:c.3539-226T>G MANE Select	NP_000543.3:n.3539-226T>G