Canonical Allele Identifier: CA383518182
Gene: VWF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6031577T>G , CM000674.2:g.6031577T>G GRCh38
NC_000012.11:g.6140743T>G , CM000674.1:g.6140743T>G GRCh37
NC_000012.10:g.6011004T>G NCBI36
NG_009072.1:g.98094A>C
NG_009072.2:g.98094A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.2687A>C MANE Select ENSP00000261405.5:p.Asp896Ala
ENST00000261405.9:c.2687A>C ENSP00000261405.5:p.Asp896Ala
ENST00000538635.5:n.421-37643A>C
NM_000552.3:c.2687A>C NP_000543.2:p.Asp896Ala
NM_000552.4:c.2687A>C NP_000543.2:p.Asp896Ala
NM_000552.5:c.2687A>C MANE Select NP_000543.3:p.Asp896Ala