Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.58624028G= , CM000673.2:g.58624028G= | GRCh38 |
| NC_000011.9:g.58391501G= , CM000673.1:g.58391501G= | GRCh37 |
| NC_000011.8:g.58148077G= | NCBI36 |
| NG_008776.1:g.6356G= | |
| NG_008776.2:g.6356G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000614.4:c.115-6G= (CNTF) MANE Select | NP_000605.1:n.115-6G= |
| ENST00000361987.6:c.115-6G= (CNTF) MANE Select | ENSP00000355370.4:n.115-6G= |
| NM_000614.3:c.115-6G= (CNTF) | NP_000605.1:n.115-6G= |
| NR_024091.1:n.1845-6G= (ZFP91-CNTF) | |
| ENST00000361987.5:c.115-6G= (CNTF) | ENSP00000355370.4:n.115-6G= |
| ENST00000389919.8:c.*87-6G= (ZFP91-CNTF) | ENSP00000455911.1:n.*87-6G= |
| ENST00000422974.2:c.1183-6G= (ZFP91-CNTF) | ENSP00000457288.1:n.1183-6G= |