Canonical Allele Identifier: CA2575053929
Gene: VWF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6023555C>T , CM000674.2:g.6023555C>T GRCh38
NC_000012.11:g.6132721C>T , CM000674.1:g.6132721C>T GRCh37
NC_000012.10:g.6002982C>T NCBI36
NG_009072.1:g.106116G>A
NG_009072.2:g.106116G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261405.10:c.3379+76G>A MANE Select ENSP00000261405.5:n.3379+76G>A
ENST00000261405.9:c.3379+76G>A ENSP00000261405.5:n.3379+76G>A
ENST00000538635.5:n.421-29621G>A
NM_000552.3:c.3379+76G>A NP_000543.2:n.3379+76G>A
NM_000552.4:c.3379+76G>A NP_000543.2:n.3379+76G>A
NM_000552.5:c.3379+76G>A MANE Select NP_000543.3:n.3379+76G>A
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