Canonical Allele Identifier: CA232298102
Gene: VWF HGNC NCBI

Linked Data

dbSNP Id: rs577172448
gnomAD v3: 12-6023549-C-A
gnomAD v4: 12-6023549-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6023549C>A , CM000674.2:g.6023549C>A GRCh38
NC_000012.11:g.6132715C>A , CM000674.1:g.6132715C>A GRCh37
NC_000012.10:g.6002976C>A NCBI36
NG_009072.1:g.106122G>T
NG_009072.2:g.106122G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261405.10:c.3379+82G>T MANE Select ENSP00000261405.5:n.3379+82G>T
ENST00000261405.9:c.3379+82G>T ENSP00000261405.5:n.3379+82G>T
ENST00000538635.5:n.421-29615G>T
NM_000552.3:c.3379+82G>T NP_000543.2:n.3379+82G>T
NM_000552.4:c.3379+82G>T NP_000543.2:n.3379+82G>T
NM_000552.5:c.3379+82G>T MANE Select NP_000543.3:n.3379+82G>T