Canonical Allele Identifier: CA2617230200

Gene: VWF

Linked Data

• gnomAD v4: 12-6022138-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6022138G>A , CM000674.2:g.6022138G>A	GRCh38
NC_000012.11:g.6131304G>A , CM000674.1:g.6131304G>A	GRCh37
NC_000012.10:g.6001565G>A	NCBI36
NG_009072.1:g.107533C>T
NG_009072.2:g.107533C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.3539-103C>T MANE Select	ENSP00000261405.5:n.3539-103C>T
ENST00000261405.9:c.3539-103C>T	ENSP00000261405.5:n.3539-103C>T
ENST00000538635.5:n.421-28204C>T
NM_000552.3:c.3539-103C>T	NP_000543.2:n.3539-103C>T
NM_000552.4:c.3539-103C>T	NP_000543.2:n.3539-103C>T
NM_000552.5:c.3539-103C>T MANE Select	NP_000543.3:n.3539-103C>T