Canonical Allele Identifier: CA383512309
Gene: VWF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6023765T>G , CM000674.2:g.6023765T>G GRCh38
NC_000012.11:g.6132931T>G , CM000674.1:g.6132931T>G GRCh37
NC_000012.10:g.6003192T>G NCBI36
NG_009072.1:g.105906A>C
NG_009072.2:g.105906A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.3245A>C MANE Select ENSP00000261405.5:p.Asp1082Ala
ENST00000261405.9:c.3245A>C ENSP00000261405.5:p.Asp1082Ala
ENST00000538635.5:n.421-29831A>C
NM_000552.3:c.3245A>C NP_000543.2:p.Asp1082Ala
NM_000552.4:c.3245A>C NP_000543.2:p.Asp1082Ala
NM_000552.5:c.3245A>C MANE Select NP_000543.3:p.Asp1082Ala