Canonical Allele Identifier: CA383512264
Gene: VWF HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.6132911A>C (hg19) chr12:g.6023745A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6023745A>C , CM000674.2:g.6023745A>C GRCh38
NC_000012.11:g.6132911A>C , CM000674.1:g.6132911A>C GRCh37
NC_000012.10:g.6003172A>C NCBI36
NG_009072.1:g.105926T>G
NG_009072.2:g.105926T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.3265T>G MANE Select ENSP00000261405.5:p.Cys1089Gly
ENST00000261405.9:c.3265T>G ENSP00000261405.5:p.Cys1089Gly
ENST00000538635.5:n.421-29811T>G
NM_000552.3:c.3265T>G NP_000543.2:p.Cys1089Gly
NM_000552.4:c.3265T>G NP_000543.2:p.Cys1089Gly
NM_000552.5:c.3265T>G MANE Select NP_000543.3:p.Cys1089Gly
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