Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94775462G= , CM000672.2:g.94775462G= | GRCh38 |
| NC_000010.10:g.96535219G= , CM000672.1:g.96535219G= | GRCh37 |
| NC_000010.9:g.96525209G= | NCBI36 |
| NG_008384.2:g.17757G= | |
| NG_008384.3:g.17782G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000371321.9:c.404G= MANE Select | ENSP00000360372.3:p.Gly135= | |
| ENST00000645461.1:n.1457G= | ||
| ENST00000371321.7:c.404G= | ENSP00000360372.3:p.Gly135= | |
| ENST00000464755.1:c.1167G= | ENSP00000483243.1:n.1167G= | |
| ENST00000480405.2:c.404G= | ENSP00000483847.1:p.Gly135= | |
| NM_000769.2:c.404G= | NP_000760.1:p.Gly135= | |
| NM_000769.4:c.404G= MANE Select | NP_000760.1:p.Gly135= |