Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.129980392T>G , CM000664.2:g.129980392T>G | GRCh38 |
| NC_000002.11:g.130737965T>G , CM000664.1:g.130737965T>G | GRCh37 |
| NC_000002.10:g.130454435T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_032144.3:c.277T>G (RAB6C) MANE Select | NP_115520.2:p.Tyr93Asp |
| ENST00000410061.4:c.277T>G (RAB6C) MANE Select | ENSP00000387307.2:p.Tyr93Asp |
| NM_032144.2:c.277T>G (RAB6C) | NP_115520.2:p.Tyr93Asp |
| NR_036537.1:n.81A>C (RAB6C-AS1) | |
| ENST00000410061.3:c.277T>G (RAB6C) | ENSP00000387307.2:p.Tyr93Asp |
| ENST00000412425.1:n.75A>C (RAB6C-AS1) | |
| ENST00000624615.1:n.21A>C (RAB6C-AS1) |