Canonical Allele Identifier: CA2013880777
Gene: VWF HGNC NCBI

Linked Data

dbSNP Id: rs1565838641
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6036136T>A , CM000674.2:g.6036136T>A GRCh38
NC_000012.11:g.6145302T>A , CM000674.1:g.6145302T>A GRCh37
NC_000012.10:g.6015563T>A NCBI36
NG_009072.1:g.93535A>T
NG_009072.2:g.93535A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.2546+252A>T MANE Select ENSP00000261405.5:n.2546+252A>T
ENST00000261405.9:c.2546+252A>T ENSP00000261405.5:n.2546+252A>T
ENST00000538635.5:n.421-42202A>T
NM_000552.3:c.2546+252A>T NP_000543.2:n.2546+252A>T
NM_000552.4:c.2546+252A>T NP_000543.2:n.2546+252A>T
NM_000552.5:c.2546+252A>T MANE Select NP_000543.3:n.2546+252A>T
Search 100 bp 5'
Search 100 bp 3'