Canonical Allele Identifier: CA6403341
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 3035020
ClinVar RCV Id: RCV004550875
dbSNP Id: rs142956629
ExAC: 12:6167193 G / A
gnomAD v2: 12-6167193-G-A
gnomAD v3: 12-6058027-G-A
gnomAD v4: 12-6058027-G-A
MyVariant Identifiers: chr12:g.6167193G>A (hg19) chr12:g.6058027G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6058027G>A , CM000674.2:g.6058027G>A GRCh38
NC_000012.11:g.6167193G>A , CM000674.1:g.6167193G>A GRCh37
NC_000012.10:g.6037454G>A NCBI36
NG_009072.1:g.71644C>T
NG_009072.2:g.71644C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.1551C>T MANE Select ENSP00000261405.5:p.Ala517=
ENST00000261405.9:c.1551C>T ENSP00000261405.5:p.Ala517=
ENST00000538635.5:n.420+52488C>T
NM_000552.3:c.1551C>T NP_000543.2:p.Ala517=
NM_000552.4:c.1551C>T NP_000543.2:p.Ala517=
NM_000552.5:c.1551C>T MANE Select NP_000543.3:p.Ala517=
Search 100 bp 5'
Search 100 bp 3'