Canonical Allele Identifier: CA383498300
Gene: VWF HGNC NCBI

Linked Data

dbSNP Id: rs1479932155
gnomAD v2: 12-6167158-C-T
gnomAD v4: 12-6057992-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6057992C>T , CM000674.2:g.6057992C>T GRCh38
NC_000012.11:g.6167158C>T , CM000674.1:g.6167158C>T GRCh37
NC_000012.10:g.6037419C>T NCBI36
NG_009072.1:g.71679G>A
NG_009072.2:g.71679G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.1586G>A MANE Select ENSP00000261405.5:p.Gly529Asp
ENST00000261405.9:c.1586G>A ENSP00000261405.5:p.Gly529Asp
ENST00000538635.5:n.420+52523G>A
NM_000552.3:c.1586G>A NP_000543.2:p.Gly529Asp
NM_000552.4:c.1586G>A NP_000543.2:p.Gly529Asp
NM_000552.5:c.1586G>A MANE Select NP_000543.3:p.Gly529Asp