Canonical Allele Identifier: CA2617230380
Gene: VWF HGNC NCBI

Linked Data

gnomAD v4: 12-6023559-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6023559C>T , CM000674.2:g.6023559C>T GRCh38
NC_000012.11:g.6132725C>T , CM000674.1:g.6132725C>T GRCh37
NC_000012.10:g.6002986C>T NCBI36
NG_009072.1:g.106112G>A
NG_009072.2:g.106112G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261405.10:c.3379+72G>A MANE Select ENSP00000261405.5:n.3379+72G>A
ENST00000261405.9:c.3379+72G>A ENSP00000261405.5:n.3379+72G>A
ENST00000538635.5:n.421-29625G>A
NM_000552.3:c.3379+72G>A NP_000543.2:n.3379+72G>A
NM_000552.4:c.3379+72G>A NP_000543.2:n.3379+72G>A
NM_000552.5:c.3379+72G>A MANE Select NP_000543.3:n.3379+72G>A
Search 100 bp 5'
Search 100 bp 3'