Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.49514328T>C , CM000679.2:g.49514328T>C | GRCh38 |
| NC_000017.10:g.47591690T>C , CM000679.1:g.47591690T>C | GRCh37 |
| NC_000017.9:g.44946689T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002507.4:c.*1319T>C (NGFR) MANE Select | NP_002498.1:n.*1319T>C |
| ENST00000172229.8:c.*1319T>C (NGFR) MANE Select | ENSP00000172229.3:n.*1319T>C |
| NM_002507.3:c.*1319T>C (NGFR) | NP_002498.1:n.*1319T>C |
| NR_103773.1:n.247-3215A>G (NGFR-AS1) | |
| ENST00000172229.7:c.*1319T>C (NGFR) | ENSP00000172229.3:n.*1319T>C |