Canonical Allele Identifier: CA478493948
Gene: VWF HGNC NCBI

Linked Data

gnomAD v4: 12-6018384-G-C
MyVariant Identifiers: chr12:g.6127550G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6018384G>C , CM000674.2:g.6018384G>C GRCh38
NC_000012.11:g.6127550G>C , CM000674.1:g.6127550G>C GRCh37
NC_000012.10:g.5997811G>C NCBI36
NG_009072.1:g.111287C>G
NG_009072.2:g.111287C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261405.10:c.5034C>G MANE Select ENSP00000261405.5:p.Pro1678=
ENST00000261405.9:c.5034C>G ENSP00000261405.5:p.Pro1678=
ENST00000538635.5:n.421-24450C>G
NM_000552.3:c.5034C>G NP_000543.2:p.Pro1678=
NM_000552.4:c.5034C>G NP_000543.2:p.Pro1678=
NM_000552.5:c.5034C>G MANE Select NP_000543.3:p.Pro1678=
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