Canonical Allele Identifier: CA690483007
Gene: VWF HGNC NCBI

Linked Data

dbSNP Id: rs1421469032
gnomAD v4: 12-6023919-A-T
MyVariant Identifiers: chr12:g.6133085A>T (hg19) chr12:g.6023919A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6023919A>T , CM000674.2:g.6023919A>T GRCh38
NC_000012.11:g.6133085A>T , CM000674.1:g.6133085A>T GRCh37
NC_000012.10:g.6003346A>T NCBI36
NG_009072.1:g.105752T>A
NG_009072.2:g.105752T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.3223-132T>A MANE Select ENSP00000261405.5:n.3223-132T>A
ENST00000261405.9:c.3223-132T>A ENSP00000261405.5:n.3223-132T>A
ENST00000538635.5:n.421-29985T>A
NM_000552.3:c.3223-132T>A NP_000543.2:n.3223-132T>A
NM_000552.4:c.3223-132T>A NP_000543.2:n.3223-132T>A
NM_000552.5:c.3223-132T>A MANE Select NP_000543.3:n.3223-132T>A
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