Canonical Allele Identifier: CA478101684
Gene: VWF HGNC NCBI

Linked Data

dbSNP Id: rs1944159041
MyVariant Identifiers: chr12:g.6132927G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6023761G>A , CM000674.2:g.6023761G>A GRCh38
NC_000012.11:g.6132927G>A , CM000674.1:g.6132927G>A GRCh37
NC_000012.10:g.6003188G>A NCBI36
NG_009072.1:g.105910C>T
NG_009072.2:g.105910C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.3249C>T MANE Select ENSP00000261405.5:p.Val1083=
ENST00000261405.9:c.3249C>T ENSP00000261405.5:p.Val1083=
ENST00000538635.5:n.421-29827C>T
NM_000552.3:c.3249C>T NP_000543.2:p.Val1083=
NM_000552.4:c.3249C>T NP_000543.2:p.Val1083=
NM_000552.5:c.3249C>T MANE Select NP_000543.3:p.Val1083=
Search 100 bp 5'
Search 100 bp 3'