Canonical Allele Identifier: CA2617230210
Gene: VWF HGNC NCBI

Linked Data

gnomAD v4: 12-6022155-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6022155C>A , CM000674.2:g.6022155C>A GRCh38
NC_000012.11:g.6131321C>A , CM000674.1:g.6131321C>A GRCh37
NC_000012.10:g.6001582C>A NCBI36
NG_009072.1:g.107516G>T
NG_009072.2:g.107516G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.3539-120G>T MANE Select ENSP00000261405.5:n.3539-120G>T
ENST00000261405.9:c.3539-120G>T ENSP00000261405.5:n.3539-120G>T
ENST00000538635.5:n.421-28221G>T
NM_000552.3:c.3539-120G>T NP_000543.2:n.3539-120G>T
NM_000552.4:c.3539-120G>T NP_000543.2:n.3539-120G>T
NM_000552.5:c.3539-120G>T MANE Select NP_000543.3:n.3539-120G>T
Search 100 bp 5'
Search 100 bp 3'