Canonical Allele Identifier: CA799777849
Gene: SNCA HGNC NCBI
SNCA-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2619363
gnomAD v3: 4-89837896-G-C
gnomAD v4: 4-89837896-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89837896G>C , CM000666.2:g.89837896G>C GRCh38
NC_000004.11:g.90759047G>C , CM000666.1:g.90759047G>C GRCh37
NC_000004.10:g.90978070G>C NCBI36
NG_011851.1:g.5401C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000336904.7:c.-26+356C>G (SNCA) ENSP00000338345.3:n.-26+356C>G
NM_001146055.1:c.-26+356C>G (SNCA) NP_001139527.1:n.-26+356C>G
NR_045481.1:n.335-365G>C (SNCA-AS1)
XM_011532205.1:c.-26+356C>G (SNCA) XP_011530507.1:n.-26+356C>G
XM_011532205.2:c.-26+356C>G (SNCA) XP_011530507.1:n.-26+356C>G
NM_001146055.2:c.-26+356C>G (SNCA) NP_001139527.1:n.-26+356C>G
NM_001375285.1:c.-95+356C>G (SNCA) NP_001362214.1:n.-95+356C>G
NR_164674.1:n.53+356C>G (SNCA)