Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.24174744C>T , CM000668.2:g.24174744C>T | GRCh38 |
| NC_000006.11:g.24174972C>T , CM000668.1:g.24174972C>T | GRCh37 |
| NC_000006.10:g.24282951C>T | NCBI36 |
| NG_012829.1:g.188309G>A | |
| NG_012829.2:g.213549G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378454.8:c.1417G>A MANE Select | ENSP00000367715.3:p.Ala473Thr | |
| ENST00000378450.6:c.676G>A | ENSP00000367711.3:p.Ala226Thr | |
| ENST00000378454.7:c.1417G>A | ENSP00000367715.3:p.Ala473Thr | |
| NM_001195610.1:c.1417G>A | NP_001182539.1:p.Ala473Thr | |
| NM_016356.4:c.1417G>A | NP_057440.2:p.Ala473Thr | |
| NM_016356.5:c.1417G>A MANE Select | NP_057440.2:p.Ala473Thr | |
| NM_001195610.2:c.1417G>A | NP_001182539.1:p.Ala473Thr |