Canonical Allele Identifier: CA383498705
Gene: VWF HGNC NCBI

Linked Data

gnomAD v4: 12-6018504-C-G
MyVariant Identifiers: chr12:g.6127670C>G (hg19) chr12:g.6018504C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6018504C>G , CM000674.2:g.6018504C>G GRCh38
NC_000012.11:g.6127670C>G , CM000674.1:g.6127670C>G GRCh37
NC_000012.10:g.5997931C>G NCBI36
NG_009072.1:g.111167G>C
NG_009072.2:g.111167G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.4914G>C MANE Select ENSP00000261405.5:p.Glu1638Asp
ENST00000261405.9:c.4914G>C ENSP00000261405.5:p.Glu1638Asp
ENST00000538635.5:n.421-24570G>C
NM_000552.3:c.4914G>C NP_000543.2:p.Glu1638Asp
NM_000552.4:c.4914G>C NP_000543.2:p.Glu1638Asp
NM_000552.5:c.4914G>C MANE Select NP_000543.3:p.Glu1638Asp
Search 100 bp 5'
Search 100 bp 3'