Canonical Allele Identifier: CA217207535
Gene: SYT9 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10769780

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.7345864T>C , CM000673.2:g.7345864T>C GRCh38
NC_000011.9:g.7367095T>C , CM000673.1:g.7367095T>C GRCh37
NC_000011.8:g.7323671T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_175733.3:c.1044+31923T>C VV NP_783860.1:p.=
XM_005252795.2:c.1044+31923T>C XP_005252852.1:p.=
XM_011519900.1:c.1044+31923T>C XP_011518202.1:p.=
XM_011519901.1:c.1044+31923T>C XP_011518203.1:p.=
XM_011519902.1:c.948+31923T>C XP_011518204.1:p.=
XM_011519903.1:c.1044+31923T>C XP_011518205.1:p.=
XM_011519904.1:c.1044+31923T>C XP_011518206.1:p.=
XM_011519905.1:c.1044+31923T>C XP_011518207.1:p.=
XM_011519900.2:c.1044+31923T>C
XM_011519901.2:c.1044+31923T>C
XM_011519902.2:c.948+31923T>C
XM_011519904.2:c.1044+31923T>C
XR_001747772.1:n.1259+31923T>C
XR_001747773.1:n.1259+31923T>C
ENST00000318881.10:c.1044+31923T>C ENSP00000324419.6:p.=
ENST00000524820.6:c.*141+31527T>C ENSP00000432141.2:p.=
ENST00000532592.1:c.497+42474T>C ENSP00000434558.1:p.=