Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.32475112C= , CM000684.2:g.32475112C= | GRCh38 |
| NC_000022.10:g.32871099C= , CM000684.1:g.32871099C= | GRCh37 |
| NC_000022.9:g.31201099C= | NCBI36 |
| NG_016001.1:g.5393C= | |
| NG_016001.2:g.5393C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266087.12:c.110C= MANE Select | ENSP00000266087.7:p.Thr37= | |
| ENST00000266087.11:c.110C= | ENSP00000266087.7:p.Thr37= | |
| ENST00000420700.5:c.110C= | ENSP00000406155.1:p.Thr37= | |
| ENST00000425028.5:c.110C= | ENSP00000395823.1:p.Thr37= | |
| ENST00000492535.1:n.98C= | ||
| NM_012179.3:c.110C= | NP_036311.3:p.Thr37= | |
| XM_011530106.1:c.-64C= | XP_011528408.1:n.-64C= | |
| XM_024452207.1:c.-81C= | XP_024307975.1:n.-81C= | |
| NM_012179.4:c.110C= MANE Select | NP_036311.3:p.Thr37= |