Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186194581T= , CM000666.2:g.186194581T= | GRCh38 |
| NC_000004.11:g.187115735T= , CM000666.1:g.187115735T= | GRCh37 |
| NC_000004.10:g.187352729T= | NCBI36 |
| NG_007965.1:g.8062T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000378802.5:c.296T= MANE Select | ENSP00000368079.4:p.Met99= | |
| ENST00000378802.4:c.296T= | ENSP00000368079.4:p.Met99= | |
| NM_207352.3:c.296T= | NP_997235.3:p.Met99= | |
| XM_005262935.2:c.296T= | XP_005262992.1:p.Met99= | |
| XM_006714184.2:c.-15T= | XP_006714247.1:n.-15T= | |
| XM_005262935.4:c.296T= | XP_005262992.1:p.Met99= | |
| XM_017008037.1:c.-15T= | XP_016863526.1:n.-15T= | |
| NM_207352.4:c.296T= MANE Select | NP_997235.3:p.Met99= |