Canonical Allele Identifier: CA478101260
Gene: VWF HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.6131134A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6021968A>T , CM000674.2:g.6021968A>T GRCh38
NC_000012.11:g.6131134A>T , CM000674.1:g.6131134A>T GRCh37
NC_000012.10:g.6001395A>T NCBI36
NG_009072.1:g.107703T>A
NG_009072.2:g.107703T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261405.10:c.3606T>A MANE Select ENSP00000261405.5:p.Ala1202=
ENST00000261405.9:c.3606T>A ENSP00000261405.5:p.Ala1202=
ENST00000538635.5:n.421-28034T>A
NM_000552.3:c.3606T>A NP_000543.2:p.Ala1202=
NM_000552.4:c.3606T>A NP_000543.2:p.Ala1202=
NM_000552.5:c.3606T>A MANE Select NP_000543.3:p.Ala1202=
Search 100 bp 5'
Search 100 bp 3'