Canonical Allele Identifier: CA383512277
Gene: VWF HGNC NCBI

Linked Data

gnomAD v4: 12-6023751-C-G
MyVariant Identifiers: chr12:g.6132917C>G (hg19) chr12:g.6023751C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6023751C>G , CM000674.2:g.6023751C>G GRCh38
NC_000012.11:g.6132917C>G , CM000674.1:g.6132917C>G GRCh37
NC_000012.10:g.6003178C>G NCBI36
NG_009072.1:g.105920G>C
NG_009072.2:g.105920G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.3259G>C MANE Select ENSP00000261405.5:p.Asp1087His
ENST00000261405.9:c.3259G>C ENSP00000261405.5:p.Asp1087His
ENST00000538635.5:n.421-29817G>C
NM_000552.3:c.3259G>C NP_000543.2:p.Asp1087His
NM_000552.4:c.3259G>C NP_000543.2:p.Asp1087His
NM_000552.5:c.3259G>C MANE Select NP_000543.3:p.Asp1087His
Search 100 bp 5'
Search 100 bp 3'