Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.45997703G= , CM000683.2:g.45997703G= | GRCh38 |
| NC_000021.8:g.47417617G= , CM000683.1:g.47417617G= | GRCh37 |
| NC_000021.7:g.46242045G= | NCBI36 |
| NG_008674.1:g.20955G= , LRG_475:g.20955G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001848.3:c.1465G= MANE Select | NP_001839.2:p.Ala489= |
| ENST00000361866.8:c.1465G= MANE Select | ENSP00000355180.3:p.Ala489= |
| NM_001848.2:c.1465G= , LRG_475t1:c.1465G= | NP_001839.2:p.Ala489= |
| ENST00000361866.7:c.1465G= | ENSP00000355180.3:p.Ala489= |
| ENST00000612273.1:c.1465G= | ENSP00000483630.1:p.Ala489= |
| ENST00000683550.1:n.240G= |