Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.15558166C>T , CM000672.2:g.15558166C>T | GRCh38 |
| NC_000010.10:g.15600165C>T , CM000672.1:g.15600165C>T | GRCh37 |
| NC_000010.9:g.15640171C>T | NCBI36 |
| NG_034116.1:g.167170G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378076.4:c.2674G>A MANE Select | ENSP00000367316.3:p.Ala892Thr | |
| ENST00000378076.3:c.2674G>A | ENSP00000367316.3:p.Ala892Thr | |
| NM_001291494.1:c.2629G>A | NP_001278423.1:p.Ala877Thr | |
| NM_003638.2:c.2674G>A | NP_003629.2:p.Ala892Thr | |
| NM_003638.3:c.2674G>A MANE Select | NP_003629.2:p.Ala892Thr | |
| NM_001291494.2:c.2629G>A | NP_001278423.1:p.Ala877Thr |