Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.17589479C>T , CM000670.2:g.17589479C>T | GRCh38 |
| NC_000008.10:g.17446988C>T , CM000670.1:g.17446988C>T | GRCh37 |
| NC_000008.9:g.17491248C>T | NCBI36 |
| NG_023332.1:g.18047C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001372073.1:c.67C>T MANE Select | NP_001359002.1:p.His23Tyr |
| ENST00000251630.11:c.67C>T MANE Select | ENSP00000251630.4:p.His23Tyr |
| NM_006207.2:c.67C>T | NP_006198.1:p.His23Tyr |
| ENST00000251630.10:c.67C>T | ENSP00000251630.4:p.His23Tyr |
| ENST00000541323.1:c.67C>T | ENSP00000444211.1:p.His23Tyr |
| ENST00000673645.1:c.67C>T | ENSP00000501219.1:p.His23Tyr |
| XM_011544558.1:c.67C>T | XP_011542860.1:p.His23Tyr |