Canonical Allele Identifier: CA383518128
Gene: VWF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6031572_6031581del , CM000674.2:g.6031572_6031581del GRCh38
NC_000012.11:g.6140738_6140747del , CM000674.1:g.6140738_6140747del GRCh37
NC_000012.10:g.6010999_6011008del NCBI36
NG_009072.1:g.98090_98099del
NG_009072.2:g.98090_98099del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.2686-3_2692del
ENST00000261405.9:c.2686-3_2692del
ENST00000538635.5:n.421-37647_421-37638del
NM_000552.3:c.2686-3_2692del
NM_000552.4:c.2686-3_2692del
NM_000552.5:c.2686-3_2692del