Canonical Allele Identifier: CA2013874861
Gene: VWF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6023640T= , CM000674.2:g.6023640T= GRCh38
NC_000012.11:g.6132806T= , CM000674.1:g.6132806T= GRCh37
NC_000012.10:g.6003067T= NCBI36
NG_009072.1:g.106031A=
NG_009072.2:g.106031A=

Transcript Alleles

HGVS Amino-acid change
ENST00000261405.10:c.3370A= MANE Select ENSP00000261405.5:p.Thr1124=
ENST00000261405.9:c.3370A= ENSP00000261405.5:p.Thr1124=
ENST00000538635.5:n.421-29706A=
NM_000552.3:c.3370A= NP_000543.2:p.Thr1124=
NM_000552.4:c.3370A= NP_000543.2:p.Thr1124=
NM_000552.5:c.3370A= MANE Select NP_000543.3:p.Thr1124=