Canonical Allele Identifier: CA383498289
Gene: VWF HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.6167152T>C (hg19) chr12:g.6057986T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6057986T>C , CM000674.2:g.6057986T>C GRCh38
NC_000012.11:g.6167152T>C , CM000674.1:g.6167152T>C GRCh37
NC_000012.10:g.6037413T>C NCBI36
NG_009072.1:g.71685A>G
NG_009072.2:g.71685A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.1592A>G MANE Select ENSP00000261405.5:p.Gln531Arg
ENST00000261405.9:c.1592A>G ENSP00000261405.5:p.Gln531Arg
ENST00000538635.5:n.420+52529A>G
NM_000552.3:c.1592A>G NP_000543.2:p.Gln531Arg
NM_000552.4:c.1592A>G NP_000543.2:p.Gln531Arg
NM_000552.5:c.1592A>G MANE Select NP_000543.3:p.Gln531Arg
Search 100 bp 5'
Search 100 bp 3'