Canonical Allele Identifier: CA383498742
Gene: VWF HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.6127687T>A (hg19) chr12:g.6018521T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6018521T>A , CM000674.2:g.6018521T>A GRCh38
NC_000012.11:g.6127687T>A , CM000674.1:g.6127687T>A GRCh37
NC_000012.10:g.5997948T>A NCBI36
NG_009072.1:g.111150A>T
NG_009072.2:g.111150A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261405.10:c.4897A>T MANE Select ENSP00000261405.5:p.Asn1633Tyr
ENST00000261405.9:c.4897A>T ENSP00000261405.5:p.Asn1633Tyr
ENST00000538635.5:n.421-24587A>T
NM_000552.3:c.4897A>T NP_000543.2:p.Asn1633Tyr
NM_000552.4:c.4897A>T NP_000543.2:p.Asn1633Tyr
NM_000552.5:c.4897A>T MANE Select NP_000543.3:p.Asn1633Tyr
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