Canonical Allele Identifier: CA2617230442
Gene: VWF HGNC NCBI

Linked Data

gnomAD v4: 12-6023883-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6023883G>T , CM000674.2:g.6023883G>T GRCh38
NC_000012.11:g.6133049G>T , CM000674.1:g.6133049G>T GRCh37
NC_000012.10:g.6003310G>T NCBI36
NG_009072.1:g.105788C>A
NG_009072.2:g.105788C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.3223-96C>A MANE Select ENSP00000261405.5:n.3223-96C>A
ENST00000261405.9:c.3223-96C>A ENSP00000261405.5:n.3223-96C>A
ENST00000538635.5:n.421-29949C>A
NM_000552.3:c.3223-96C>A NP_000543.2:n.3223-96C>A
NM_000552.4:c.3223-96C>A NP_000543.2:n.3223-96C>A
NM_000552.5:c.3223-96C>A MANE Select NP_000543.3:n.3223-96C>A
Search 100 bp 5'
Search 100 bp 3'