Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.67753901C= , CM000666.2:g.67753901C= | GRCh38 |
| NC_000004.11:g.68619619C= , CM000666.1:g.68619619C= | GRCh37 |
| NC_000004.10:g.68302214C= | NCBI36 |
| NG_009293.1:g.7186G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000226413.5:c.435G= MANE Select | ENSP00000226413.5:p.Arg145= | |
| ENST00000226413.4:c.435G= | ENSP00000226413.4:p.Arg145= | |
| ENST00000420975.2:c.435G= | ENSP00000397561.2:p.Arg145= | |
| NM_000406.2:c.435G= | NP_000397.1:p.Arg145= | |
| NM_001012763.1:c.435G= | NP_001012781.1:p.Arg145= | |
| NM_000406.3:c.435G= MANE Select | NP_000397.1:p.Arg145= | |
| NM_001012763.2:c.435G= | NP_001012781.1:p.Arg145= |