Canonical Allele Identifier: CA919013591
Gene: VWF HGNC NCBI

Linked Data

dbSNP Id: rs1555194658

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6016234_6016516del , CM000674.2:g.6016234_6016516del GRCh38
NC_000012.11:g.6125400_6125682del , CM000674.1:g.6125400_6125682del GRCh37
NC_000012.10:g.5995661_5995943del NCBI36
NG_009072.1:g.113157_113439del
NG_009072.2:g.113157_113439del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.5311+2_5312del
ENST00000261405.9:c.5311+2_5312del
ENST00000538635.5:n.421-22580_421-22298del
NM_000552.3:c.5311+2_5312del
NM_000552.4:c.5311+2_5312del
NM_000552.5:c.5311+2_5312del