Canonical Allele Identifier: CA383506209
Gene: VWF HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.6128665G>C (hg19) chr12:g.6019499G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6019499G>C , CM000674.2:g.6019499G>C GRCh38
NC_000012.11:g.6128665G>C , CM000674.1:g.6128665G>C GRCh37
NC_000012.10:g.5998926G>C NCBI36
NG_009072.1:g.110172C>G
NG_009072.2:g.110172C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261405.10:c.3919C>G MANE Select ENSP00000261405.5:p.Leu1307Val
ENST00000261405.9:c.3919C>G ENSP00000261405.5:p.Leu1307Val
ENST00000538635.5:n.421-25565C>G
NM_000552.3:c.3919C>G NP_000543.2:p.Leu1307Val
NM_000552.4:c.3919C>G NP_000543.2:p.Leu1307Val
NM_000552.5:c.3919C>G MANE Select NP_000543.3:p.Leu1307Val
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