Canonical Allele Identifier: CA232310581
Gene: VWF HGNC NCBI

Linked Data

dbSNP Id: rs912452327
gnomAD v3: 12-6057902-C-G
gnomAD v4: 12-6057902-C-G
MyVariant Identifiers: chr12:g.6167068C>G (hg19) chr12:g.6057902C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6057902C>G , CM000674.2:g.6057902C>G GRCh38
NC_000012.11:g.6167068C>G , CM000674.1:g.6167068C>G GRCh37
NC_000012.10:g.6037329C>G NCBI36
NG_009072.1:g.71769G>C
NG_009072.2:g.71769G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.1676G>C MANE Select ENSP00000261405.5:p.Cys559Ser
ENST00000261405.9:c.1676G>C ENSP00000261405.5:p.Cys559Ser
ENST00000538635.5:n.420+52613G>C
NM_000552.3:c.1676G>C NP_000543.2:p.Cys559Ser
NM_000552.4:c.1676G>C NP_000543.2:p.Cys559Ser
NM_000552.5:c.1676G>C MANE Select NP_000543.3:p.Cys559Ser
Search 100 bp 5'
Search 100 bp 3'