Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48367512C= , CM000675.2:g.48367512C= | GRCh38 |
| NC_000013.10:g.48941648C= , CM000675.1:g.48941648C= | GRCh37 |
| NC_000013.9:g.47839649C= | NCBI36 |
| NG_009009.1:g.68766C= , LRG_517:g.68766C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000321.3:c.958C= MANE Select | NP_000312.2:p.Arg320= |
| ENST00000267163.6:c.958C= MANE Select | ENSP00000267163.4:p.Arg320= |
| NM_000321.2:c.958C= , LRG_517t1:c.958C= | NP_000312.2:p.Arg320= |
| ENST00000267163.4:c.958C= | ENSP00000267163.4:p.Arg320= |
| ENST00000650461.1:c.958C= | ENSP00000497193.1:p.Arg320= |
| XM_011535171.1:c.697C= | XP_011533473.1:p.Arg233= |
| XM_011535171.2:c.697C= | XP_011533473.1:p.Arg233= |
| XR_002957522.1:n.122-2536G= |