Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.41756696C>G , CM000683.2:g.41756696C>G | GRCh38 |
| NC_000021.8:g.43176856C>G , CM000683.1:g.43176856C>G | GRCh37 |
| NC_000021.7:g.42049925C>G | NCBI36 |
| NG_032113.1:g.15394G>C | |
| NG_032113.2:g.15394G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000332512.8:c.303G>C MANE Select | ENSP00000332454.3:p.Thr101= | |
| ENST00000332512.7:c.303G>C | ENSP00000332454.3:p.Thr101= | |
| ENST00000352483.3:c.303G>C | ENSP00000330161.2:p.Thr101= | |
| NM_020639.2:c.303G>C | NP_065690.2:p.Thr101= | |
| NM_020639.3:c.303G>C MANE Select | NP_065690.2:p.Thr101= |