Canonical Allele Identifier: CA2013849734
Gene: VWF HGNC NCBI

Linked Data

dbSNP Id: rs1591835552
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5968869A>G , CM000674.2:g.5968869A>G GRCh38
NC_000012.11:g.6078035A>G , CM000674.1:g.6078035A>G GRCh37
NC_000012.10:g.5948296A>G NCBI36
NG_009072.1:g.160802T>C
NG_009072.2:g.160802T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261405.10:c.7729+342T>C MANE Select ENSP00000261405.5:n.7729+342T>C
ENST00000261405.9:c.7729+342T>C ENSP00000261405.5:n.7729+342T>C
NM_000552.3:c.7729+342T>C NP_000543.2:n.7729+342T>C
NM_000552.4:c.7729+342T>C NP_000543.2:n.7729+342T>C
NM_000552.5:c.7729+342T>C MANE Select NP_000543.3:n.7729+342T>C
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