Canonical Allele Identifier: CA383498002
Gene: VWF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6057879T>C , CM000674.2:g.6057879T>C GRCh38
NC_000012.11:g.6167045T>C , CM000674.1:g.6167045T>C GRCh37
NC_000012.10:g.6037306T>C NCBI36
NG_009072.1:g.71792A>G
NG_009072.2:g.71792A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.1699A>G MANE Select ENSP00000261405.5:p.Ser567Gly
ENST00000261405.9:c.1699A>G ENSP00000261405.5:p.Ser567Gly
ENST00000538635.5:n.420+52636A>G
NM_000552.3:c.1699A>G NP_000543.2:p.Ser567Gly
NM_000552.4:c.1699A>G NP_000543.2:p.Ser567Gly
NM_000552.5:c.1699A>G MANE Select NP_000543.3:p.Ser567Gly