Canonical Allele Identifier: CA2013849781
Gene: VWF HGNC NCBI

Linked Data

dbSNP Id: rs1943436958
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5968968G>A , CM000674.2:g.5968968G>A GRCh38
NC_000012.11:g.6078134G>A , CM000674.1:g.6078134G>A GRCh37
NC_000012.10:g.5948395G>A NCBI36
NG_009072.1:g.160703C>T
NG_009072.2:g.160703C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.7729+243C>T MANE Select ENSP00000261405.5:n.7729+243C>T
ENST00000261405.9:c.7729+243C>T ENSP00000261405.5:n.7729+243C>T
NM_000552.3:c.7729+243C>T NP_000543.2:n.7729+243C>T
NM_000552.4:c.7729+243C>T NP_000543.2:n.7729+243C>T
NM_000552.5:c.7729+243C>T MANE Select NP_000543.3:n.7729+243C>T
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