Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.129980134T>C , CM000664.2:g.129980134T>C | GRCh38 |
| NC_000002.11:g.130737707T>C , CM000664.1:g.130737707T>C | GRCh37 |
| NC_000002.10:g.130454177T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_032144.3:c.19T>C (RAB6C) MANE Select | NP_115520.2:p.Phe7Leu |
| ENST00000410061.4:c.19T>C (RAB6C) MANE Select | ENSP00000387307.2:p.Phe7Leu |
| NM_032144.2:c.19T>C (RAB6C) | NP_115520.2:p.Phe7Leu |
| NR_036537.1:n.225A>G (RAB6C-AS1) | |
| ENST00000410061.3:c.19T>C (RAB6C) | ENSP00000387307.2:p.Phe7Leu |
| ENST00000412425.1:n.219A>G (RAB6C-AS1) | |
| ENST00000624615.1:n.279A>G (RAB6C-AS1) |