Canonical Allele Identifier: CA478101240

Gene: VWF

Linked Data

• MyVariant Identifiers: chr12:g.6131113T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6021947T>G , CM000674.2:g.6021947T>G	GRCh38
NC_000012.11:g.6131113T>G , CM000674.1:g.6131113T>G	GRCh37
NC_000012.10:g.6001374T>G	NCBI36
NG_009072.1:g.107724A>C
NG_009072.2:g.107724A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.3627A>C MANE Select	ENSP00000261405.5:p.Gly1209=
ENST00000261405.9:c.3627A>C	ENSP00000261405.5:p.Gly1209=
ENST00000538635.5:n.421-28013A>C
NM_000552.3:c.3627A>C	NP_000543.2:p.Gly1209=
NM_000552.4:c.3627A>C	NP_000543.2:p.Gly1209=
NM_000552.5:c.3627A>C MANE Select	NP_000543.3:p.Gly1209=