Canonical Allele Identifier: CA1475334051
Gene: SNCA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89718399G= , CM000666.2:g.89718399G= GRCh38
NC_000004.11:g.90639550G= , CM000666.1:g.90639550G= GRCh37
NC_000004.10:g.90858573G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000673902.1:c.390+10795C= ENSP00000501102.1:n.390+10795C=
XR_938982.1:n.3490-1427G=
XR_938984.1:n.2890-1427G=
XR_938985.1:n.1922-1427G=
XR_938986.1:n.556-1427G=
XR_938987.1:n.810-1427G=
XR_938988.1:n.676-1427G=
XR_938989.1:n.332-1427G=
XR_938990.1:n.420-1427G=
XR_938991.1:n.435-1427G=
XR_938993.1:n.437-1427G=
XR_938994.1:n.901-1427G=
XR_938995.1:n.735-1427G=
XR_001741765.1:n.2908-1427G=
XR_001741766.1:n.1680-1427G=
XR_938982.2:n.3490-1427G=
XR_938984.2:n.2912-1427G=
XR_938985.2:n.1944-1427G=
XR_938986.2:n.581-1427G=
XR_938987.2:n.870-1427G=
XR_938989.2:n.354-1427G=