Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.148827642G>T , CM000667.2:g.148827642G>T | GRCh38 |
| NC_000005.9:g.148207205G>T , CM000667.1:g.148207205G>T | GRCh37 |
| NC_000005.8:g.148187398G>T | NCBI36 |
| NG_016421.1:g.6050G>T | |
| NG_016421.2:g.6050G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000305988.6:c.811G>T MANE Select | ENSP00000305372.4:p.Ala271Ser | |
| ENST00000305988.5:c.811G>T | ENSP00000305372.4:p.Ala271Ser | |
| NM_000024.5:c.811G>T | NP_000015.1:p.Ala271Ser | |
| NM_000024.6:c.811G>T MANE Select | NP_000015.2:p.Ala271Ser |