Canonical Allele Identifier: CA2013874939
Gene: VWF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6023769G= , CM000674.2:g.6023769G= GRCh38
NC_000012.11:g.6132935G= , CM000674.1:g.6132935G= GRCh37
NC_000012.10:g.6003196G= NCBI36
NG_009072.1:g.105902C=
NG_009072.2:g.105902C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.3241C= MANE Select ENSP00000261405.5:p.Leu1081=
ENST00000261405.9:c.3241C= ENSP00000261405.5:p.Leu1081=
ENST00000538635.5:n.421-29835C=
NM_000552.3:c.3241C= NP_000543.2:p.Leu1081=
NM_000552.4:c.3241C= NP_000543.2:p.Leu1081=
NM_000552.5:c.3241C= MANE Select NP_000543.3:p.Leu1081=