Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154863160C= , CM000685.2:g.154863160C= | GRCh38 |
| NC_000023.10:g.154091435C= , CM000685.1:g.154091435C= | GRCh37 |
| NC_000023.9:g.153744629C= | NCBI36 |
| NG_011403.1:g.164564G= | |
| NG_011403.2:g.164564G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.6497G= MANE Select | ENSP00000353393.4:p.Arg2166= | |
| ENST00000644698.1:c.230G= | ENSP00000495706.1:p.Arg77= | |
| ENST00000330287.10:c.92G= | ENSP00000327895.6:p.Arg31= | |
| ENST00000360256.8:c.6497G= | ENSP00000353393.4:p.Arg2166= | |
| NM_000132.3:c.6497G= | NP_000123.1:p.Arg2166= | |
| NM_019863.2:c.92G= | NP_063916.1:p.Arg31= | |
| XM_011531126.1:c.6392G= | XP_011529428.1:p.Arg2131= | |
| NM_000132.4:c.6497G= MANE Select | NP_000123.1:p.Arg2166= | |
| NM_019863.3:c.92G= | NP_063916.1:p.Arg31= |