Canonical Allele Identifier: CA11784315
Gene: SNCA HGNC NCBI
SNCA-AS1 HGNC NCBI
MyVariant.info:
GRCh38 chr4:g.89837238G>C
GRCh37 chr4:g.90758389G>C
gnomAD v2:
4:90758389 G / C
gnomAD v3:
4:89837238 G / C
gnomAD v4:
chr4-89837238-G-C
Joint Max Group AF 0.8300152 (EAS)
Genomes Max Group AF 0.82978119 (EAS)
Exomes Max Group AF 0.58171467 (EAS)
dbSNP:
2301135
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89837238G>C , CM000666.2:g.89837238G>C GRCh38
NC_000004.11:g.90758389G>C , CM000666.1:g.90758389G>C GRCh37
NC_000004.10:g.90977412G>C NCBI36
NG_011851.1:g.6059C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000673902.1:c.-302C>G (SNCA) ENSP00000501102.1:n.-302C>G
ENST00000674129.1:c.-302C>G (SNCA) ENSP00000501269.1:n.-302C>G
ENST00000336904.7:c.-26+1014C>G (SNCA) ENSP00000338345.3:n.-26+1014C>G
NM_001146055.1:c.-26+1014C>G (SNCA) NP_001139527.1:n.-26+1014C>G
NR_045481.1:n.334+504G>C (SNCA-AS1)
XM_011532205.1:c.-26+1014C>G (SNCA) XP_011530507.1:n.-26+1014C>G
XM_011532205.2:c.-26+1014C>G (SNCA) XP_011530507.1:n.-26+1014C>G
NM_001146055.2:c.-26+1014C>G (SNCA) NP_001139527.1:n.-26+1014C>G
NM_001375285.1:c.-94-709C>G (SNCA) NP_001362214.1:n.-94-709C>G
NR_164674.1:n.53+1014C>G (SNCA)
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