Canonical Allele Identifier: CA232298885
Gene: VWF HGNC NCBI

Linked Data

dbSNP Id: rs569303699
gnomAD v3: 12-6031722-G-C
gnomAD v4: 12-6031722-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6031722G>C , CM000674.2:g.6031722G>C GRCh38
NC_000012.11:g.6140888G>C , CM000674.1:g.6140888G>C GRCh37
NC_000012.10:g.6011149G>C NCBI36
NG_009072.1:g.97949C>G
NG_009072.2:g.97949C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.2686-144C>G MANE Select ENSP00000261405.5:n.2686-144C>G
ENST00000261405.9:c.2686-144C>G ENSP00000261405.5:n.2686-144C>G
ENST00000538635.5:n.421-37788C>G
NM_000552.3:c.2686-144C>G NP_000543.2:n.2686-144C>G
NM_000552.4:c.2686-144C>G NP_000543.2:n.2686-144C>G
NM_000552.5:c.2686-144C>G MANE Select NP_000543.3:n.2686-144C>G