Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.113588287G= , CM000672.2:g.113588287G= | GRCh38 |
| NC_000010.10:g.115348046G= , CM000672.1:g.115348046G= | GRCh37 |
| NC_000010.9:g.115338036G= | NCBI36 |
| NG_008956.1:g.40269G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004132.5:c.1601G= MANE Select | NP_004123.1:p.Gly534= |
| ENST00000351270.4:c.1601G= MANE Select | ENSP00000277903.4:p.Gly534= |
| NM_001177660.1:c.1523G= | NP_001171131.1:p.Gly508= |
| NM_001177660.2:c.1523G= | NP_001171131.1:p.Gly508= |
| NM_001177660.3:c.1523G= | NP_001171131.1:p.Gly508= |
| NM_004132.3:c.1601G= | NP_004123.1:p.Gly534= |
| NM_004132.4:c.1601G= | NP_004123.1:p.Gly534= |
| ENST00000351270.3:c.1601G= | ENSP00000277903.4:p.Gly534= |
| ENST00000542051.5:c.1523G= | ENSP00000443283.1:p.Gly508= |