Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.49508983T= , CM000679.2:g.49508983T= | GRCh38 |
| NC_000017.10:g.47586345T= , CM000679.1:g.47586345T= | GRCh37 |
| NC_000017.9:g.44941344T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000172229.8:c.569-1429T= (NGFR) MANE Select | ENSP00000172229.3:n.569-1429T= | |
| ENST00000172229.7:c.569-1429T= (NGFR) | ENSP00000172229.3:n.569-1429T= | |
| ENST00000504201.1:c.287-1429T= (NGFR) | ENSP00000421731.1:n.287-1429T= | |
| NM_002507.3:c.569-1429T= (NGFR) | NP_002498.1:n.569-1429T= | |
| NR_103773.1:n.377+2000A= (NGFR-AS1) | ||
| NM_002507.4:c.569-1429T= (NGFR) MANE Select | NP_002498.1:n.569-1429T= |