Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94775426T= , CM000672.2:g.94775426T= | GRCh38 |
| NC_000010.10:g.96535183T= , CM000672.1:g.96535183T= | GRCh37 |
| NC_000010.9:g.96525173T= | NCBI36 |
| NG_008384.2:g.17721T= | |
| NG_008384.3:g.17746T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371321.9:c.368T= MANE Select | ENSP00000360372.3:p.Ile123= | |
| ENST00000645461.1:n.1421T= | ||
| ENST00000371321.7:c.368T= | ENSP00000360372.3:p.Ile123= | |
| ENST00000464755.1:c.1131T= | ENSP00000483243.1:n.1131T= | |
| ENST00000480405.2:c.368T= | ENSP00000483847.1:p.Ile123= | |
| NM_000769.2:c.368T= | NP_000760.1:p.Ile123= | |
| NM_000769.4:c.368T= MANE Select | NP_000760.1:p.Ile123= |