Canonical Allele Identifier: CA6402804

Gene: VWF

Linked Data

• dbSNP Id: rs4021577
• ExAC: 12:6133000 G / A
• gnomAD v2: 12-6133000-G-A
• gnomAD v3: 12-6023834-G-A
• gnomAD v4: 12-6023834-G-A
• MyVariant Identifiers: chr12:g.6133000G>A (hg19) ; chr12:g.6023834G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6023834G>A , CM000674.2:g.6023834G>A	GRCh38
NC_000012.11:g.6133000G>A , CM000674.1:g.6133000G>A	GRCh37
NC_000012.10:g.6003261G>A	NCBI36
NG_009072.1:g.105837C>T
NG_009072.2:g.105837C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.3223-47C>T MANE Select	ENSP00000261405.5:n.3223-47C>T
ENST00000261405.9:c.3223-47C>T	ENSP00000261405.5:n.3223-47C>T
ENST00000538635.5:n.421-29900C>T
NM_000552.3:c.3223-47C>T	NP_000543.2:n.3223-47C>T
NM_000552.4:c.3223-47C>T	NP_000543.2:n.3223-47C>T
NM_000552.5:c.3223-47C>T MANE Select	NP_000543.3:n.3223-47C>T