Canonical Allele Identifier: CA228862

Gene: VWF

Linked Data

• ClinVar Variation Id: 100512
• ClinVar RCV Id: RCV000086927 ; RCV001787087 ; RCV002243756 ; RCV002280872
• dbSNP Id: rs61754000
• ExAC: 12:6182812 G / A
• gnomAD v2: 12-6182812-G-A
• gnomAD v3: 12-6073646-G-A
• gnomAD v4: 12-6073646-G-A
• MyVariant Identifiers: chr12:g.6182812G>A (hg19) ; chr12:g.6073646G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6073646G>A , CM000674.2:g.6073646G>A	GRCh38
NC_000012.11:g.6182812G>A , CM000674.1:g.6182812G>A	GRCh37
NC_000012.10:g.6053073G>A	NCBI36
NG_009072.1:g.56025C>T
NG_009072.2:g.56025C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.970C>T MANE Select	ENSP00000261405.5:p.Arg324Ter
ENST00000261405.9:c.970C>T	ENSP00000261405.5:p.Arg324Ter
ENST00000538635.5:n.420+36869C>T
NM_000552.3:c.970C>T	NP_000543.2:p.Arg324Ter
NM_000552.4:c.970C>T	NP_000543.2:p.Arg324Ter
NM_000552.5:c.970C>T MANE Select	NP_000543.3:p.Arg324Ter