Canonical Allele Identifier: CA6402715
Gene: VWF HGNC NCBI

Linked Data

dbSNP Id: rs754106010
ExAC: 12:6131035 T / A
gnomAD v2: 12-6131035-T-A
gnomAD v3: 12-6021869-T-A
gnomAD v4: 12-6021869-T-A
MyVariant Identifiers: chr12:g.6131035T>A (hg19) chr12:g.6021869T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6021869T>A , CM000674.2:g.6021869T>A GRCh38
NC_000012.11:g.6131035T>A , CM000674.1:g.6131035T>A GRCh37
NC_000012.10:g.6001296T>A NCBI36
NG_009072.1:g.107802A>T
NG_009072.2:g.107802A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261405.10:c.3674+31A>T MANE Select ENSP00000261405.5:n.3674+31A>T
ENST00000261405.9:c.3674+31A>T ENSP00000261405.5:n.3674+31A>T
ENST00000538635.5:n.421-27935A>T
ENST00000539641.1:n.27+31A>T
NM_000552.3:c.3674+31A>T NP_000543.2:n.3674+31A>T
NM_000552.4:c.3674+31A>T NP_000543.2:n.3674+31A>T
NM_000552.5:c.3674+31A>T MANE Select NP_000543.3:n.3674+31A>T
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