Canonical Allele Identifier: CA1475385661
Gene: SNCA HGNC NCBI
SNCA-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1739592268

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89837873C>G , CM000666.2:g.89837873C>G GRCh38
NC_000004.11:g.90759024C>G , CM000666.1:g.90759024C>G GRCh37
NC_000004.10:g.90978047C>G NCBI36
NG_011851.1:g.5424G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000336904.7:c.-26+379G>C (SNCA) ENSP00000338345.3:n.-26+379G>C
NM_001146055.1:c.-26+379G>C (SNCA) NP_001139527.1:n.-26+379G>C
NR_045481.1:n.335-388C>G (SNCA-AS1)
XM_011532205.1:c.-26+379G>C (SNCA) XP_011530507.1:n.-26+379G>C
XM_011532205.2:c.-26+379G>C (SNCA) XP_011530507.1:n.-26+379G>C
NM_001146055.2:c.-26+379G>C (SNCA) NP_001139527.1:n.-26+379G>C
NM_001375285.1:c.-95+379G>C (SNCA) NP_001362214.1:n.-95+379G>C
NR_164674.1:n.53+379G>C (SNCA)