Canonical Allele Identifier: CA2013872464
Gene: VWF HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6018339C= , CM000674.2:g.6018339C= GRCh38
NC_000012.11:g.6127505C= , CM000674.1:g.6127505C= GRCh37
NC_000012.10:g.5997766C= NCBI36
NG_009072.1:g.111332G=
NG_009072.2:g.111332G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.5053+26G= MANE Select ENSP00000261405.5:n.5053+26G=
ENST00000261405.9:c.5053+26G= ENSP00000261405.5:n.5053+26G=
ENST00000538635.5:n.421-24405G=
NM_000552.3:c.5053+26G= NP_000543.2:n.5053+26G=
NM_000552.4:c.5053+26G= NP_000543.2:n.5053+26G=
NM_000552.5:c.5053+26G= MANE Select NP_000543.3:n.5053+26G=
Search 100 bp 5'
Search 100 bp 3'