Canonical Allele Identifier: CA2013849754
Gene: VWF HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5968914G= , CM000674.2:g.5968914G= GRCh38
NC_000012.11:g.6078080G= , CM000674.1:g.6078080G= GRCh37
NC_000012.10:g.5948341G= NCBI36
NG_009072.1:g.160757C=
NG_009072.2:g.160757C=

Transcript Alleles

HGVS Amino-acid change
ENST00000261405.10:c.7729+297C= MANE Select ENSP00000261405.5:n.7729+297C=
ENST00000261405.9:c.7729+297C= ENSP00000261405.5:n.7729+297C=
NM_000552.3:c.7729+297C= NP_000543.2:n.7729+297C=
NM_000552.4:c.7729+297C= NP_000543.2:n.7729+297C=
NM_000552.5:c.7729+297C= MANE Select NP_000543.3:n.7729+297C=
Search 100 bp 5'
Search 100 bp 3'