Canonical Allele Identifier: CA15780658
Gene: VWA8 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1900442

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.41931538T>C , CM000675.2:g.41931538T>C GRCh38
NC_000013.10:g.42505674T>C , CM000675.1:g.42505674T>C GRCh37
NC_000013.9:g.41403674T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001009814.1:c.241+18398A>G VV NP_001009814.1:p.=
NM_015058.1:c.241+18398A>G VV NP_055873.1:p.=
XM_011535006.1:c.-48+18398A>G XP_011533308.1:p.=
XM_011535007.1:c.241+18398A>G XP_011533309.1:p.=
XM_011535007.3:c.241+18398A>G XP_011533309.1:p.=
XM_017020469.2:c.58+5777A>G XP_016875958.1:p.=
XM_017020470.2:c.241+18398A>G XP_016875959.1:p.=
XM_017020471.2:c.241+18398A>G XP_016875960.1:p.=
XM_017020474.2:c.241+18398A>G XP_016875963.1:p.=
XR_001749518.2:n.972+18398A>G
ENST00000281496.6:c.241+18398A>G ENSP00000281496.6:p.=
ENST00000379310.7:c.241+18398A>G ENSP00000368612.3:p.=