Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.40866783C>G , CM000679.2:g.40866783C>G | GRCh38 |
| NC_000017.10:g.39023035C>G , CM000679.1:g.39023035C>G | GRCh37 |
| NC_000017.9:g.36276561C>G | NCBI36 |
| NG_008077.1:g.5428G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251643.5:c.404G>C MANE Select | ENSP00000251643.4:p.Arg135Thr | |
| ENST00000647902.1:c.296G>C | ENSP00000497770.1:p.Arg99Thr | |
| ENST00000251643.4:c.404G>C | ENSP00000251643.4:p.Arg135Thr | |
| NM_000223.3:c.404G>C | NP_000214.1:p.Arg135Thr | |
| XR_934754.1:n.1500+15923C>G | ||
| XR_934754.2:n.2008+15923C>G | ||
| NM_000223.4:c.404G>C MANE Select | NP_000214.1:p.Arg135Thr |