Canonical Allele Identifier: CA478101538
Gene: VWF HGNC NCBI

Linked Data

gnomAD v4: 12-6023668-A-G
MyVariant Identifiers: chr12:g.6132834A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6023668A>G , CM000674.2:g.6023668A>G GRCh38
NC_000012.11:g.6132834A>G , CM000674.1:g.6132834A>G GRCh37
NC_000012.10:g.6003095A>G NCBI36
NG_009072.1:g.106003T>C
NG_009072.2:g.106003T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.3342T>C MANE Select ENSP00000261405.5:p.His1114=
ENST00000261405.9:c.3342T>C ENSP00000261405.5:p.His1114=
ENST00000538635.5:n.421-29734T>C
NM_000552.3:c.3342T>C NP_000543.2:p.His1114=
NM_000552.4:c.3342T>C NP_000543.2:p.His1114=
NM_000552.5:c.3342T>C MANE Select NP_000543.3:p.His1114=
Search 100 bp 5'
Search 100 bp 3'