Canonical Allele Identifier: CA1139532066
Gene: VWF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6023777_6023797dup , CM000674.2:g.6023777_6023797dup GRCh38
NC_000012.11:g.6132943_6132963dup , CM000674.1:g.6132943_6132963dup GRCh37
NC_000012.10:g.6003204_6003224dup NCBI36
NG_009072.1:g.105877_105897dup
NG_009072.2:g.105877_105897dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.3223-7_3236dup
ENST00000261405.9:c.3223-7_3236dup
ENST00000538635.5:n.421-29860_421-29840dup
NM_000552.3:c.3223-7_3236dup
NM_000552.4:c.3223-7_3236dup
NM_000552.5:c.3223-7_3236dup