Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128344398T= , CM000667.2:g.128344398T= | GRCh38 |
| NC_000005.9:g.127680090T= , CM000667.1:g.127680090T= | GRCh37 |
| NC_000005.8:g.127707989T= | NCBI36 |
| NG_008750.1:g.198646A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262464.9:c.3330A= MANE Select | ENSP00000262464.4:p.Glu1110= | |
| ENST00000262464.8:c.3330A= | ENSP00000262464.4:p.Glu1110= | |
| ENST00000508053.5:c.3330A= | ENSP00000424571.1:p.Glu1110= | |
| ENST00000508989.5:c.3231A= | ENSP00000425596.1:p.Glu1077= | |
| ENST00000619499.4:c.3327A= | ENSP00000482132.1:p.Glu1109= | |
| NM_001999.3:c.3330A= | NP_001990.2:p.Glu1110= | |
| XM_017009228.2:c.3177A= | XP_016864717.1:p.Glu1059= | |
| NM_001999.4:c.3330A= MANE Select | NP_001990.2:p.Glu1110= |