Canonical Allele Identifier: CA2013876937
Gene: VWF HGNC NCBI

Linked Data

dbSNP Id: rs1944266114
gnomAD v3: 12-6031732-G-A
gnomAD v4: 12-6031732-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6031732G>A , CM000674.2:g.6031732G>A GRCh38
NC_000012.11:g.6140898G>A , CM000674.1:g.6140898G>A GRCh37
NC_000012.10:g.6011159G>A NCBI36
NG_009072.1:g.97939C>T
NG_009072.2:g.97939C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.2686-154C>T MANE Select ENSP00000261405.5:n.2686-154C>T
ENST00000261405.9:c.2686-154C>T ENSP00000261405.5:n.2686-154C>T
ENST00000538635.5:n.421-37798C>T
NM_000552.3:c.2686-154C>T NP_000543.2:n.2686-154C>T
NM_000552.4:c.2686-154C>T NP_000543.2:n.2686-154C>T
NM_000552.5:c.2686-154C>T MANE Select NP_000543.3:n.2686-154C>T
Search 100 bp 5'
Search 100 bp 3'