Canonical Allele Identifier: CA478103022
Gene: VWF HGNC NCBI

Linked Data

dbSNP Id: rs1358017451
gnomAD v2: 12-6143977-C-A
MyVariant Identifiers: chr12:g.6143977C>A (hg19) chr12:g.6034811C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6034811C>A , CM000674.2:g.6034811C>A GRCh38
NC_000012.11:g.6143977C>A , CM000674.1:g.6143977C>A GRCh37
NC_000012.10:g.6014238C>A NCBI36
NG_009072.1:g.94860G>T
NG_009072.2:g.94860G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.2562G>T MANE Select ENSP00000261405.5:p.Arg854=
ENST00000261405.9:c.2562G>T ENSP00000261405.5:p.Arg854=
ENST00000538635.5:n.421-40877G>T
NM_000552.3:c.2562G>T NP_000543.2:p.Arg854=
NM_000552.4:c.2562G>T NP_000543.2:p.Arg854=
NM_000552.5:c.2562G>T MANE Select NP_000543.3:p.Arg854=
Search 100 bp 5'
Search 100 bp 3'