Canonical Allele Identifier: CA1630855478
Gene: VWF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6058030A= , CM000674.2:g.6058030A= GRCh38
NC_000012.11:g.6167196A= , CM000674.1:g.6167196A= GRCh37
NC_000012.10:g.6037457A= NCBI36
NG_009072.1:g.71641T=
NG_009072.2:g.71641T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.1548T= MANE Select ENSP00000261405.5:p.Tyr516=
ENST00000261405.9:c.1548T= ENSP00000261405.5:p.Tyr516=
ENST00000538635.5:n.420+52485T=
NM_000552.3:c.1548T= NP_000543.2:p.Tyr516=
NM_000552.4:c.1548T= NP_000543.2:p.Tyr516=
NM_000552.5:c.1548T= MANE Select NP_000543.3:p.Tyr516=