HGVS | Genome Assembly |
---|---|
NC_000004.12:g.89837905A>G , CM000666.2:g.89837905A>G | GRCh38 |
NC_000004.11:g.90759056A>G , CM000666.1:g.90759056A>G | GRCh37 |
NC_000004.10:g.90978079A>G | NCBI36 |
NG_011851.1:g.5392T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000336904.7:c.-26+347T>C (SNCA) | ENSP00000338345.3:n.-26+347T>C | |
NM_001146055.1:c.-26+347T>C (SNCA) | NP_001139527.1:n.-26+347T>C | |
NR_045481.1:n.335-356A>G (SNCA-AS1) | ||
XM_011532205.1:c.-26+347T>C (SNCA) | XP_011530507.1:n.-26+347T>C | |
XM_011532205.2:c.-26+347T>C (SNCA) | XP_011530507.1:n.-26+347T>C | |
NM_001146055.2:c.-26+347T>C (SNCA) | NP_001139527.1:n.-26+347T>C | |
NM_001375285.1:c.-95+347T>C (SNCA) | NP_001362214.1:n.-95+347T>C | |
NR_164674.1:n.53+347T>C (SNCA) |