Canonical Allele Identifier: CA383497853
Gene: VWF HGNC NCBI

Linked Data

dbSNP Id: rs1728851627
gnomAD v4: 12-6057857-G-A
MyVariant Identifiers: chr12:g.6167023G>A (hg19) chr12:g.6057857G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6057857G>A , CM000674.2:g.6057857G>A GRCh38
NC_000012.11:g.6167023G>A , CM000674.1:g.6167023G>A GRCh37
NC_000012.10:g.6037284G>A NCBI36
NG_009072.1:g.71814C>T
NG_009072.2:g.71814C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.1721C>T MANE Select ENSP00000261405.5:p.Pro574Leu
ENST00000261405.9:c.1721C>T ENSP00000261405.5:p.Pro574Leu
ENST00000538635.5:n.420+52658C>T
NM_000552.3:c.1721C>T NP_000543.2:p.Pro574Leu
NM_000552.4:c.1721C>T NP_000543.2:p.Pro574Leu
NM_000552.5:c.1721C>T MANE Select NP_000543.3:p.Pro574Leu
Search 100 bp 5'
Search 100 bp 3'