Canonical Allele Identifier: CA2013849784
Gene: VWF HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5968972C= , CM000674.2:g.5968972C= GRCh38
NC_000012.11:g.6078138C= , CM000674.1:g.6078138C= GRCh37
NC_000012.10:g.5948399C= NCBI36
NG_009072.1:g.160699G=
NG_009072.2:g.160699G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.7729+239G= MANE Select ENSP00000261405.5:n.7729+239G=
ENST00000261405.9:c.7729+239G= ENSP00000261405.5:n.7729+239G=
NM_000552.3:c.7729+239G= NP_000543.2:n.7729+239G=
NM_000552.4:c.7729+239G= NP_000543.2:n.7729+239G=
NM_000552.5:c.7729+239G= MANE Select NP_000543.3:n.7729+239G=
Search 100 bp 5'
Search 100 bp 3'