Canonical Allele Identifier: CA478493946
Gene: VWF HGNC NCBI

Linked Data

gnomAD v4: 12-6018381-G-T
MyVariant Identifiers: chr12:g.6127547G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6018381G>T , CM000674.2:g.6018381G>T GRCh38
NC_000012.11:g.6127547G>T , CM000674.1:g.6127547G>T GRCh37
NC_000012.10:g.5997808G>T NCBI36
NG_009072.1:g.111290C>A
NG_009072.2:g.111290C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.5037C>A MANE Select ENSP00000261405.5:p.Thr1679=
ENST00000261405.9:c.5037C>A ENSP00000261405.5:p.Thr1679=
ENST00000538635.5:n.421-24447C>A
NM_000552.3:c.5037C>A NP_000543.2:p.Thr1679=
NM_000552.4:c.5037C>A NP_000543.2:p.Thr1679=
NM_000552.5:c.5037C>A MANE Select NP_000543.3:p.Thr1679=
Search 100 bp 5'
Search 100 bp 3'