Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.202467682A= , CM000664.2:g.202467682A= | GRCh38 |
| NC_000002.11:g.203332405A= , CM000664.1:g.203332405A= | GRCh37 |
| NC_000002.10:g.203040650A= | NCBI36 |
| NG_009363.1:g.96356A= , LRG_712:g.96356A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374580.10:c.411A= MANE Select | ENSP00000363708.4:p.Thr137= | |
| ENST00000638587.1:c.342A= | ENSP00000491062.1:p.Thr114= | |
| ENST00000374574.2:c.411A= | ENSP00000363702.2:p.Thr137= | |
| ENST00000374580.8:c.411A= | ENSP00000363708.4:p.Thr137= | |
| ENST00000479069.1:n.318A= | ||
| NM_001204.6:c.411A= , LRG_712t1:c.411A= | NP_001195.2:p.Thr137= | |
| XM_011511687.1:c.411A= | XP_011509989.1:p.Thr137= | |
| XM_011511688.1:c.411A= | XP_011509990.1:p.Thr137= | |
| NM_001204.7:c.411A= MANE Select | NP_001195.2:p.Thr137= |