Linked Data
MyVariant Identifiers:
chr10:g.50819422T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.49611376T>G , CM000672.2:g.49611376T>G | GRCh38 |
| NC_000010.10:g.50819422T>G , CM000672.1:g.50819422T>G | GRCh37 |
| NC_000010.9:g.50489428T>G | NCBI36 |
| NG_011797.1:g.7282T>G | |
| NG_053144.1:g.6076T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374115.5:c.636T>G (SLC18A3) MANE Select | ENSP00000363229.3:p.Arg212= | |
| ENST00000339797.5:c.-69+2177T>G (CHAT) | ENSP00000343486.1:n.-69+2177T>G | |
| ENST00000374115.4:c.636T>G (SLC18A3) | ENSP00000363229.3:p.Arg212= | |
| NM_003055.2:c.636T>G (SLC18A3) | NP_003046.2:p.Arg212= | |
| NM_020984.3:c.-69+2177T>G (CHAT) | NP_066264.3:n.-69+2177T>G | |
| NM_003055.3:c.636T>G (SLC18A3) MANE Select | NP_003046.2:p.Arg212= | |
| NM_020984.4:c.-69+2177T>G (CHAT) | NP_066264.4:n.-69+2177T>G |