Canonical Allele Identifier: CA2013880758

Gene: VWF

Linked Data

• dbSNP Id: rs1305005674

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6036079C>A , CM000674.2:g.6036079C>A	GRCh38
NC_000012.11:g.6145245C>A , CM000674.1:g.6145245C>A	GRCh37
NC_000012.10:g.6015506C>A	NCBI36
NG_009072.1:g.93592G>T
NG_009072.2:g.93592G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.2546+309G>T MANE Select	ENSP00000261405.5:n.2546+309G>T
ENST00000261405.9:c.2546+309G>T	ENSP00000261405.5:n.2546+309G>T
ENST00000538635.5:n.421-42145G>T
NM_000552.3:c.2546+309G>T	NP_000543.2:n.2546+309G>T
NM_000552.4:c.2546+309G>T	NP_000543.2:n.2546+309G>T
NM_000552.5:c.2546+309G>T MANE Select	NP_000543.3:n.2546+309G>T