Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.89837939A>G , CM000666.2:g.89837939A>G | GRCh38 |
| NC_000004.11:g.90759090A>G , CM000666.1:g.90759090A>G | GRCh37 |
| NC_000004.10:g.90978113A>G | NCBI36 |
| NG_011851.1:g.5358T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000336904.7:c.-26+313T>C (SNCA) | ENSP00000338345.3:n.-26+313T>C | |
| NM_001146055.1:c.-26+313T>C (SNCA) | NP_001139527.1:n.-26+313T>C | |
| NR_045481.1:n.335-322A>G (SNCA-AS1) | ||
| XM_011532205.1:c.-26+313T>C (SNCA) | XP_011530507.1:n.-26+313T>C | |
| XM_011532205.2:c.-26+313T>C (SNCA) | XP_011530507.1:n.-26+313T>C | |
| NM_001146055.2:c.-26+313T>C (SNCA) | NP_001139527.1:n.-26+313T>C | |
| NM_001375285.1:c.-95+313T>C (SNCA) | NP_001362214.1:n.-95+313T>C | |
| NR_164674.1:n.53+313T>C (SNCA) |