Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154928831C= , CM000685.2:g.154928831C= | GRCh38 |
| NC_000023.10:g.154157106C= , CM000685.1:g.154157106C= | GRCh37 |
| NC_000023.9:g.153810300C= | NCBI36 |
| NG_011403.1:g.98893G= | |
| NG_011403.2:g.98893G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.4959G= MANE Select | ENSP00000353393.4:p.Arg1653= | |
| ENST00000360256.8:c.4959G= | ENSP00000353393.4:p.Arg1653= | |
| NM_000132.3:c.4959G= | NP_000123.1:p.Arg1653= | |
| XM_011531126.1:c.4854G= | XP_011529428.1:p.Arg1618= | |
| NM_000132.4:c.4959G= MANE Select | NP_000123.1:p.Arg1653= |