Canonical Allele Identifier: CA478104085

Gene: VWF

Linked Data

• MyVariant Identifiers: chr12:g.6167184G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6058018G>T , CM000674.2:g.6058018G>T	GRCh38
NC_000012.11:g.6167184G>T , CM000674.1:g.6167184G>T	GRCh37
NC_000012.10:g.6037445G>T	NCBI36
NG_009072.1:g.71653C>A
NG_009072.2:g.71653C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.1560C>A MANE Select	ENSP00000261405.5:p.Thr520=
ENST00000261405.9:c.1560C>A	ENSP00000261405.5:p.Thr520=
ENST00000538635.5:n.420+52497C>A
NM_000552.3:c.1560C>A	NP_000543.2:p.Thr520=
NM_000552.4:c.1560C>A	NP_000543.2:p.Thr520=
NM_000552.5:c.1560C>A MANE Select	NP_000543.3:p.Thr520=