Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.17376276C>T , CM000685.2:g.17376276C>T | GRCh38 |
| NC_000023.10:g.17394399C>T , CM000685.1:g.17394399C>T | GRCh37 |
| NC_000023.9:g.17304320C>T | NCBI36 |
| NG_011553.2:g.5857C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001291867.2:c.519C>T MANE Select | NP_001278796.1:p.Gly173= |
| ENST00000676302.1:c.519C>T MANE Select | ENSP00000502262.1:p.Gly173= |
| NM_001291867.1:c.519C>T | NP_001278796.1:p.Gly173= |
| NM_198270.3:c.519C>T | NP_938011.1:p.Gly173= |
| NM_198270.4:c.519C>T | NP_938011.1:p.Gly173= |
| ENST00000380060.7:c.519C>T | ENSP00000369400.3:p.Gly173= |