Canonical Allele Identifier: CA915940276

Gene: VWF

Linked Data

• ClinVar Variation Id: 1698781
• ClinVar RCV Id: RCV002272638
• dbSNP Id: rs61748495

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6025901C>G , CM000674.2:g.6025901C>G	GRCh38
NC_000012.11:g.6135067C>G , CM000674.1:g.6135067C>G	GRCh37
NC_000012.10:g.6005328C>G	NCBI36
NG_009072.1:g.103770G>C
NG_009072.2:g.103770G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261405.10:c.3108+5G>C MANE Select	ENSP00000261405.5:n.3108+5G>C
ENST00000261405.9:c.3108+5G>C	ENSP00000261405.5:n.3108+5G>C
ENST00000538635.5:n.421-31967G>C
NM_000552.3:c.3108+5G>C	NP_000543.2:n.3108+5G>C
NM_000552.4:c.3108+5G>C	NP_000543.2:n.3108+5G>C
NM_000552.5:c.3108+5G>C MANE Select	NP_000543.3:n.3108+5G>C