Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.123034406T= , CM000672.2:g.123034406T= | GRCh38 |
| NC_000010.10:g.124793922T= , CM000672.1:g.124793922T= | GRCh37 |
| NC_000010.9:g.124783912T= | NCBI36 |
| NG_008003.1:g.30494T= , LRG_451:g.30494T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358776.7:c.93T= MANE Select | ENSP00000357873.3:p.His31= | |
| ENST00000358776.6:c.93T= | ENSP00000357873.3:p.His31= | |
| ENST00000368869.8:c.-113T= | ENSP00000357862.4:n.-113T= | |
| ENST00000411816.2:n.110T= | ||
| NM_001609.3:c.93T= , LRG_451t1:c.93T= | NP_001600.1:p.His31= | |
| NM_001330174.1:c.-113T= | NP_001317103.1:n.-113T= | |
| NM_001330174.2:c.-113T= | NP_001317103.1:n.-113T= | |
| NM_001609.4:c.93T= MANE Select | NP_001600.1:p.His31= | |
| NM_001330174.3:c.-113T= | NP_001317103.1:n.-113T= |