Canonical Allele Identifier: CA2013874821
Gene: VWF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6023561C= , CM000674.2:g.6023561C= GRCh38
NC_000012.11:g.6132727C= , CM000674.1:g.6132727C= GRCh37
NC_000012.10:g.6002988C= NCBI36
NG_009072.1:g.106110G=
NG_009072.2:g.106110G=

Transcript Alleles

HGVS Amino-acid change
ENST00000261405.10:c.3379+70G= MANE Select ENSP00000261405.5:n.3379+70G=
ENST00000261405.9:c.3379+70G= ENSP00000261405.5:n.3379+70G=
ENST00000538635.5:n.421-29627G=
NM_000552.3:c.3379+70G= NP_000543.2:n.3379+70G=
NM_000552.4:c.3379+70G= NP_000543.2:n.3379+70G=
NM_000552.5:c.3379+70G= MANE Select NP_000543.3:n.3379+70G=