Canonical Allele Identifier: CA2013884491
Gene: VWF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6044197G= , CM000674.2:g.6044197G= GRCh38
NC_000012.11:g.6153363G= , CM000674.1:g.6153363G= GRCh37
NC_000012.10:g.6023624G= NCBI36
NG_009072.1:g.85474C=
NG_009072.2:g.85474C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.2442+94C= MANE Select ENSP00000261405.5:n.2442+94C=
ENST00000261405.9:c.2442+94C= ENSP00000261405.5:n.2442+94C=
ENST00000538635.5:n.421-50263C=
NM_000552.3:c.2442+94C= NP_000543.2:n.2442+94C=
NM_000552.4:c.2442+94C= NP_000543.2:n.2442+94C=
NM_000552.5:c.2442+94C= MANE Select NP_000543.3:n.2442+94C=
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