Canonical Allele Identifier: CA2725481764

Gene: VWF

Linked Data

• dbSNP Id: rs2136440122

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6044212T>C , CM000674.2:g.6044212T>C	GRCh38
NC_000012.11:g.6153378T>C , CM000674.1:g.6153378T>C	GRCh37
NC_000012.10:g.6023639T>C	NCBI36
NG_009072.1:g.85459A>G
NG_009072.2:g.85459A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.2442+79A>G MANE Select	ENSP00000261405.5:n.2442+79A>G
ENST00000261405.9:c.2442+79A>G	ENSP00000261405.5:n.2442+79A>G
ENST00000538635.5:n.421-50278A>G
NM_000552.3:c.2442+79A>G	NP_000543.2:n.2442+79A>G
NM_000552.4:c.2442+79A>G	NP_000543.2:n.2442+79A>G
NM_000552.5:c.2442+79A>G MANE Select	NP_000543.3:n.2442+79A>G