Canonical Allele Identifier: CA2617230458
Gene: VWF HGNC NCBI

Linked Data

gnomAD v4: 12-6023898-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6023898G>T , CM000674.2:g.6023898G>T GRCh38
NC_000012.11:g.6133064G>T , CM000674.1:g.6133064G>T GRCh37
NC_000012.10:g.6003325G>T NCBI36
NG_009072.1:g.105773C>A
NG_009072.2:g.105773C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.3223-111C>A MANE Select ENSP00000261405.5:n.3223-111C>A
ENST00000261405.9:c.3223-111C>A ENSP00000261405.5:n.3223-111C>A
ENST00000538635.5:n.421-29964C>A
NM_000552.3:c.3223-111C>A NP_000543.2:n.3223-111C>A
NM_000552.4:c.3223-111C>A NP_000543.2:n.3223-111C>A
NM_000552.5:c.3223-111C>A MANE Select NP_000543.3:n.3223-111C>A
Search 100 bp 5'
Search 100 bp 3'