Canonical Allele Identifier: CA478102765

Gene: VWF

Linked Data

• dbSNP Id: rs1555195984
• MyVariant Identifiers: chr12:g.6140737_6140746del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6031571_6031580del , CM000674.2:g.6031571_6031580del	GRCh38
NC_000012.11:g.6140737_6140746del , CM000674.1:g.6140737_6140746del	GRCh37
NC_000012.10:g.6010998_6011007del	NCBI36
NG_009072.1:g.98091_98100del
NG_009072.2:g.98091_98100del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.2686-2_2693del
ENST00000261405.9:c.2686-2_2693del
ENST00000538635.5:n.421-37646_421-37637del
NM_000552.3:c.2686-2_2693del
NM_000552.4:c.2686-2_2693del
NM_000552.5:c.2686-2_2693del