Canonical Allele Identifier: CA2013876923
Gene: VWF HGNC NCBI

Linked Data

dbSNP Id: rs569303699
gnomAD v4: 12-6031722-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6031722G>A , CM000674.2:g.6031722G>A GRCh38
NC_000012.11:g.6140888G>A , CM000674.1:g.6140888G>A GRCh37
NC_000012.10:g.6011149G>A NCBI36
NG_009072.1:g.97949C>T
NG_009072.2:g.97949C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.2686-144C>T MANE Select ENSP00000261405.5:n.2686-144C>T
ENST00000261405.9:c.2686-144C>T ENSP00000261405.5:n.2686-144C>T
ENST00000538635.5:n.421-37788C>T
NM_000552.3:c.2686-144C>T NP_000543.2:n.2686-144C>T
NM_000552.4:c.2686-144C>T NP_000543.2:n.2686-144C>T
NM_000552.5:c.2686-144C>T MANE Select NP_000543.3:n.2686-144C>T
Search 100 bp 5'
Search 100 bp 3'