Canonical Allele Identifier: CA2013884528
Gene: VWF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6044285A= , CM000674.2:g.6044285A= GRCh38
NC_000012.11:g.6153451A= , CM000674.1:g.6153451A= GRCh37
NC_000012.10:g.6023712A= NCBI36
NG_009072.1:g.85386T=
NG_009072.2:g.85386T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.2442+6T= MANE Select ENSP00000261405.5:n.2442+6T=
ENST00000261405.9:c.2442+6T= ENSP00000261405.5:n.2442+6T=
ENST00000538635.5:n.421-50351T=
NM_000552.3:c.2442+6T= NP_000543.2:n.2442+6T=
NM_000552.4:c.2442+6T= NP_000543.2:n.2442+6T=
NM_000552.5:c.2442+6T= MANE Select NP_000543.3:n.2442+6T=
Search 100 bp 5'
Search 100 bp 3'