Canonical Allele Identifier: CA383511954
Gene: VWF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6023660A>C , CM000674.2:g.6023660A>C GRCh38
NC_000012.11:g.6132826A>C , CM000674.1:g.6132826A>C GRCh37
NC_000012.10:g.6003087A>C NCBI36
NG_009072.1:g.106011T>G
NG_009072.2:g.106011T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.3350T>G MANE Select ENSP00000261405.5:p.Val1117Gly
ENST00000261405.9:c.3350T>G ENSP00000261405.5:p.Val1117Gly
ENST00000538635.5:n.421-29726T>G
NM_000552.3:c.3350T>G NP_000543.2:p.Val1117Gly
NM_000552.4:c.3350T>G NP_000543.2:p.Val1117Gly
NM_000552.5:c.3350T>G MANE Select NP_000543.3:p.Val1117Gly