Canonical Allele Identifier: CA2617231619

Gene: VWF

Linked Data

• gnomAD v4: 12-6044171-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6044171T>A , CM000674.2:g.6044171T>A	GRCh38
NC_000012.11:g.6153337T>A , CM000674.1:g.6153337T>A	GRCh37
NC_000012.10:g.6023598T>A	NCBI36
NG_009072.1:g.85500A>T
NG_009072.2:g.85500A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.2442+120A>T MANE Select	ENSP00000261405.5:n.2442+120A>T
ENST00000261405.9:c.2442+120A>T	ENSP00000261405.5:n.2442+120A>T
ENST00000538635.5:n.421-50237A>T
NM_000552.3:c.2442+120A>T	NP_000543.2:n.2442+120A>T
NM_000552.4:c.2442+120A>T	NP_000543.2:n.2442+120A>T
NM_000552.5:c.2442+120A>T MANE Select	NP_000543.3:n.2442+120A>T