Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154152987A= , CM000685.2:g.154152987A= | GRCh38 |
| NG_009105.2:g.13737A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_020061.6:c.457A= MANE Select | NP_064445.2:p.Met153= |
| ENST00000369951.9:c.457A= MANE Select | ENSP00000358967.4:p.Met153= |
| NM_020061.5:c.457A= | NP_064445.2:p.Met153= |
| ENST00000369951.8:c.457A= | ENSP00000358967.4:p.Met153= |
| ENST00000442922.1:c.46A= | ENSP00000402493.1:p.Met16= |
| ENST00000463296.1:n.467A= |