Canonical Allele Identifier: CA383518173
Gene: VWF HGNC NCBI

Linked Data

dbSNP Id: rs1239647717
gnomAD v2: 12-6140741-A-G
MyVariant Identifiers: chr12:g.6140741A>G (hg19) chr12:g.6031575A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6031575A>G , CM000674.2:g.6031575A>G GRCh38
NC_000012.11:g.6140741A>G , CM000674.1:g.6140741A>G GRCh37
NC_000012.10:g.6011002A>G NCBI36
NG_009072.1:g.98096T>C
NG_009072.2:g.98096T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.2689T>C MANE Select ENSP00000261405.5:p.Tyr897His
ENST00000261405.9:c.2689T>C ENSP00000261405.5:p.Tyr897His
ENST00000538635.5:n.421-37641T>C
NM_000552.3:c.2689T>C NP_000543.2:p.Tyr897His
NM_000552.4:c.2689T>C NP_000543.2:p.Tyr897His
NM_000552.5:c.2689T>C MANE Select NP_000543.3:p.Tyr897His
Search 100 bp 5'
Search 100 bp 3'