Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.178994825C>G , CM000667.2:g.178994825C>G | GRCh38 |
| NC_000005.9:g.178421826C>G , CM000667.1:g.178421826C>G | GRCh37 |
| NC_000005.8:g.178354432C>G | NCBI36 |
| NG_008105.1:g.5299G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000517717.3:c.120G>C MANE Select | ENSP00000430767.1:p.Thr40= | |
| ENST00000650031.1:c.120G>C | ENSP00000497110.1:p.Thr40= | |
| ENST00000231188.9:c.120G>C | ENSP00000231188.5:p.Thr40= | |
| ENST00000517717.1:c.120G>C | ENSP00000430767.1:p.Thr40= | |
| NM_000843.3:c.120G>C | NP_000834.2:p.Thr40= | |
| NM_000843.4:c.120G>C MANE Select | NP_000834.2:p.Thr40= |