Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94775182G= , CM000672.2:g.94775182G= | GRCh38 |
| NC_000010.10:g.96534939G= , CM000672.1:g.96534939G= | GRCh37 |
| NC_000010.9:g.96524929G= | NCBI36 |
| NG_008384.2:g.17477G= | |
| NG_008384.3:g.17502G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371321.9:c.293G= MANE Select | ENSP00000360372.3:p.Gly98= | |
| ENST00000645461.1:n.1346G= | ||
| ENST00000371321.7:c.293G= | ENSP00000360372.3:p.Gly98= | |
| ENST00000464755.1:c.1056G= | ENSP00000483243.1:n.1056G= | |
| ENST00000480405.2:c.293G= | ENSP00000483847.1:p.Gly98= | |
| NM_000769.2:c.293G= | NP_000760.1:p.Gly98= | |
| NM_000769.4:c.293G= MANE Select | NP_000760.1:p.Gly98= |