Canonical Allele Identifier: CA2013892384
Gene: VWF HGNC NCBI

Linked Data

dbSNP Id: rs1944611058
gnomAD v4: 12-6058131-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6058131A>C , CM000674.2:g.6058131A>C GRCh38
NC_000012.11:g.6167297A>C , CM000674.1:g.6167297A>C GRCh37
NC_000012.10:g.6037558A>C NCBI36
NG_009072.1:g.71540T>G
NG_009072.2:g.71540T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.1534-87T>G MANE Select ENSP00000261405.5:n.1534-87T>G
ENST00000261405.9:c.1534-87T>G ENSP00000261405.5:n.1534-87T>G
ENST00000538635.5:n.420+52384T>G
NM_000552.3:c.1534-87T>G NP_000543.2:n.1534-87T>G
NM_000552.4:c.1534-87T>G NP_000543.2:n.1534-87T>G
NM_000552.5:c.1534-87T>G MANE Select NP_000543.3:n.1534-87T>G
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