Canonical Allele Identifier: CA2013880788

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6036154G= , CM000674.2:g.6036154G=	GRCh38
NC_000012.11:g.6145320G= , CM000674.1:g.6145320G=	GRCh37
NC_000012.10:g.6015581G=	NCBI36
NG_009072.1:g.93517C=
NG_009072.2:g.93517C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.2546+234C= MANE Select	ENSP00000261405.5:n.2546+234C=
ENST00000261405.9:c.2546+234C=	ENSP00000261405.5:n.2546+234C=
ENST00000538635.5:n.421-42220C=
NM_000552.3:c.2546+234C=	NP_000543.2:n.2546+234C=
NM_000552.4:c.2546+234C=	NP_000543.2:n.2546+234C=
NM_000552.5:c.2546+234C= MANE Select	NP_000543.3:n.2546+234C=