Canonical Allele Identifier: CA2013880896
Gene: VWF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6036361C= , CM000674.2:g.6036361C= GRCh38
NC_000012.11:g.6145527C= , CM000674.1:g.6145527C= GRCh37
NC_000012.10:g.6015788C= NCBI36
NG_009072.1:g.93310G=
NG_009072.2:g.93310G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.2546+27G= MANE Select ENSP00000261405.5:n.2546+27G=
ENST00000261405.9:c.2546+27G= ENSP00000261405.5:n.2546+27G=
ENST00000538635.5:n.421-42427G=
NM_000552.3:c.2546+27G= NP_000543.2:n.2546+27G=
NM_000552.4:c.2546+27G= NP_000543.2:n.2546+27G=
NM_000552.5:c.2546+27G= MANE Select NP_000543.3:n.2546+27G=