Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19966884A>T , CM000670.2:g.19966884A>T | GRCh38 |
| NC_000008.10:g.19824395A>T , CM000670.1:g.19824395A>T | GRCh37 |
| NC_000008.9:g.19868675A>T | NCBI36 |
| NG_008855.1:g.32814A>T | |
| NG_008855.2:g.70168A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000650287.1:c.*1574A>T MANE Select | ENSP00000497642.1:n.*1574A>T | |
| ENST00000650478.1:c.1942A>T | ENSP00000497560.1:n.1942A>T | |
| ENST00000311322.8:c.*1574A>T | ENSP00000309757.6:n.*1574A>T | |
| NM_000237.2:c.*1574A>T | NP_000228.1:n.*1574A>T | |
| NM_000237.3:c.*1574A>T MANE Select | NP_000228.1:n.*1574A>T |