Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.49514247T>G , CM000679.2:g.49514247T>G | GRCh38 |
| NC_000017.10:g.47591609T>G , CM000679.1:g.47591609T>G | GRCh37 |
| NC_000017.9:g.44946608T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002507.4:c.*1238T>G (NGFR) MANE Select | NP_002498.1:n.*1238T>G |
| ENST00000172229.8:c.*1238T>G (NGFR) MANE Select | ENSP00000172229.3:n.*1238T>G |
| NM_002507.3:c.*1238T>G (NGFR) | NP_002498.1:n.*1238T>G |
| NR_103773.1:n.247-3134A>C (NGFR-AS1) | |
| ENST00000172229.7:c.*1238T>G (NGFR) | ENSP00000172229.3:n.*1238T>G |