Canonical Allele Identifier: CA2541742649

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6036036A>C , CM000674.2:g.6036036A>C	GRCh38
NC_000012.11:g.6145202A>C , CM000674.1:g.6145202A>C	GRCh37
NC_000012.10:g.6015463A>C	NCBI36
NG_009072.1:g.93635T>G
NG_009072.2:g.93635T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.2546+352T>G MANE Select	ENSP00000261405.5:n.2546+352T>G
ENST00000261405.9:c.2546+352T>G	ENSP00000261405.5:n.2546+352T>G
ENST00000538635.5:n.421-42102T>G
NM_000552.3:c.2546+352T>G	NP_000543.2:n.2546+352T>G
NM_000552.4:c.2546+352T>G	NP_000543.2:n.2546+352T>G
NM_000552.5:c.2546+352T>G MANE Select	NP_000543.3:n.2546+352T>G