Canonical Allele Identifier: CA2741226412

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6031734G>C , CM000674.2:g.6031734G>C	GRCh38
NC_000012.11:g.6140900G>C , CM000674.1:g.6140900G>C	GRCh37
NC_000012.10:g.6011161G>C	NCBI36
NG_009072.1:g.97937C>G
NG_009072.2:g.97937C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.2686-156C>G MANE Select	ENSP00000261405.5:n.2686-156C>G
ENST00000261405.9:c.2686-156C>G	ENSP00000261405.5:n.2686-156C>G
ENST00000538635.5:n.421-37800C>G
NM_000552.3:c.2686-156C>G	NP_000543.2:n.2686-156C>G
NM_000552.4:c.2686-156C>G	NP_000543.2:n.2686-156C>G
NM_000552.5:c.2686-156C>G MANE Select	NP_000543.3:n.2686-156C>G