Canonical Allele Identifier: CA232298096
Gene: VWF HGNC NCBI

Linked Data

dbSNP Id: rs537168070
gnomAD v3: 12-6023530-T-C
gnomAD v4: 12-6023530-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6023530T>C , CM000674.2:g.6023530T>C GRCh38
NC_000012.11:g.6132696T>C , CM000674.1:g.6132696T>C GRCh37
NC_000012.10:g.6002957T>C NCBI36
NG_009072.1:g.106141A>G
NG_009072.2:g.106141A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261405.10:c.3379+101A>G MANE Select ENSP00000261405.5:n.3379+101A>G
ENST00000261405.9:c.3379+101A>G ENSP00000261405.5:n.3379+101A>G
ENST00000538635.5:n.421-29596A>G
NM_000552.3:c.3379+101A>G NP_000543.2:n.3379+101A>G
NM_000552.4:c.3379+101A>G NP_000543.2:n.3379+101A>G
NM_000552.5:c.3379+101A>G MANE Select NP_000543.3:n.3379+101A>G