Canonical Allele Identifier: CA2617232780
Gene: VWF HGNC NCBI

Linked Data

gnomAD v4: 12-6058172-A-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6058172A>T , CM000674.2:g.6058172A>T GRCh38
NC_000012.11:g.6167338A>T , CM000674.1:g.6167338A>T GRCh37
NC_000012.10:g.6037599A>T NCBI36
NG_009072.1:g.71499T>A
NG_009072.2:g.71499T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.1534-128T>A MANE Select ENSP00000261405.5:n.1534-128T>A
ENST00000261405.9:c.1534-128T>A ENSP00000261405.5:n.1534-128T>A
ENST00000538635.5:n.420+52343T>A
NM_000552.3:c.1534-128T>A NP_000543.2:n.1534-128T>A
NM_000552.4:c.1534-128T>A NP_000543.2:n.1534-128T>A
NM_000552.5:c.1534-128T>A MANE Select NP_000543.3:n.1534-128T>A
Search 100 bp 5'
Search 100 bp 3'