Canonical Allele Identifier: CA2617230417
Gene: VWF HGNC NCBI

Linked Data

gnomAD v4: 12-6023832-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6023832A>C , CM000674.2:g.6023832A>C GRCh38
NC_000012.11:g.6132998A>C , CM000674.1:g.6132998A>C GRCh37
NC_000012.10:g.6003259A>C NCBI36
NG_009072.1:g.105839T>G
NG_009072.2:g.105839T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.3223-45T>G MANE Select ENSP00000261405.5:n.3223-45T>G
ENST00000261405.9:c.3223-45T>G ENSP00000261405.5:n.3223-45T>G
ENST00000538635.5:n.421-29898T>G
NM_000552.3:c.3223-45T>G NP_000543.2:n.3223-45T>G
NM_000552.4:c.3223-45T>G NP_000543.2:n.3223-45T>G
NM_000552.5:c.3223-45T>G MANE Select NP_000543.3:n.3223-45T>G
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