Canonical Allele Identifier: CA2013874058
Gene: VWF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6021861A= , CM000674.2:g.6021861A= GRCh38
NC_000012.11:g.6131027A= , CM000674.1:g.6131027A= GRCh37
NC_000012.10:g.6001288A= NCBI36
NG_009072.1:g.107810T=
NG_009072.2:g.107810T=

Transcript Alleles

HGVS Amino-acid change
ENST00000261405.10:c.3674+39T= MANE Select ENSP00000261405.5:n.3674+39T=
ENST00000261405.9:c.3674+39T= ENSP00000261405.5:n.3674+39T=
ENST00000538635.5:n.421-27927T=
ENST00000539641.1:n.27+39T=
NM_000552.3:c.3674+39T= NP_000543.2:n.3674+39T=
NM_000552.4:c.3674+39T= NP_000543.2:n.3674+39T=
NM_000552.5:c.3674+39T= MANE Select NP_000543.3:n.3674+39T=
Search 100 bp 5'
Search 100 bp 3'