Canonical Allele Identifier: CA2575053880
Gene: VWF HGNC NCBI

Linked Data

gnomAD v4: 12-6018313-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6018313C>T , CM000674.2:g.6018313C>T GRCh38
NC_000012.11:g.6127479C>T , CM000674.1:g.6127479C>T GRCh37
NC_000012.10:g.5997740C>T NCBI36
NG_009072.1:g.111358G>A
NG_009072.2:g.111358G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.5053+52G>A MANE Select ENSP00000261405.5:n.5053+52G>A
ENST00000261405.9:c.5053+52G>A ENSP00000261405.5:n.5053+52G>A
ENST00000538635.5:n.421-24379G>A
NM_000552.3:c.5053+52G>A NP_000543.2:n.5053+52G>A
NM_000552.4:c.5053+52G>A NP_000543.2:n.5053+52G>A
NM_000552.5:c.5053+52G>A MANE Select NP_000543.3:n.5053+52G>A
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