Canonical Allele Identifier: CA383511755
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 1065300
ClinVar RCV Id: RCV001787218
dbSNP Id: rs2136418281
MyVariant Identifiers: chr12:g.6132795A>G (hg19) chr12:g.6023629A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6023629A>G , CM000674.2:g.6023629A>G GRCh38
NC_000012.11:g.6132795A>G , CM000674.1:g.6132795A>G GRCh37
NC_000012.10:g.6003056A>G NCBI36
NG_009072.1:g.106042T>C
NG_009072.2:g.106042T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.3379+2T>C MANE Select ENSP00000261405.5:n.3379+2T>C
ENST00000261405.9:c.3379+2T>C ENSP00000261405.5:n.3379+2T>C
ENST00000538635.5:n.421-29695T>C
NM_000552.3:c.3379+2T>C NP_000543.2:n.3379+2T>C
NM_000552.4:c.3379+2T>C NP_000543.2:n.3379+2T>C
NM_000552.5:c.3379+2T>C MANE Select NP_000543.3:n.3379+2T>C
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