Canonical Allele Identifier: CA383498453

Gene: VWF

Linked Data

• MyVariant Identifiers: chr12:g.6127549T>A (hg19) ; chr12:g.6018383T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6018383T>A , CM000674.2:g.6018383T>A	GRCh38
NC_000012.11:g.6127549T>A , CM000674.1:g.6127549T>A	GRCh37
NC_000012.10:g.5997810T>A	NCBI36
NG_009072.1:g.111288A>T
NG_009072.2:g.111288A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.5035A>T MANE Select	ENSP00000261405.5:p.Thr1679Ser
ENST00000261405.9:c.5035A>T	ENSP00000261405.5:p.Thr1679Ser
ENST00000538635.5:n.421-24449A>T
NM_000552.3:c.5035A>T	NP_000543.2:p.Thr1679Ser
NM_000552.4:c.5035A>T	NP_000543.2:p.Thr1679Ser
NM_000552.5:c.5035A>T MANE Select	NP_000543.3:p.Thr1679Ser