Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67435652A= , CM000678.2:g.67435652A= | GRCh38 |
| NC_000016.9:g.67469555A= , CM000678.1:g.67469555A= | GRCh37 |
| NC_000016.8:g.66027056A= | NCBI36 |
| NG_016549.1:g.9520A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000326152.6:c.290A= MANE Select | ENSP00000316786.5:p.Glu97= | |
| ENST00000326152.5:c.290A= | ENSP00000316786.5:p.Glu97= | |
| ENST00000566606.1:c.268A= | ENSP00000473429.1:n.268A= | |
| ENST00000567684.2:n.153A= | ||
| NM_000196.3:c.290A= | NP_000187.3:p.Glu97= | |
| NM_000196.4:c.290A= MANE Select | NP_000187.3:p.Glu97= |