Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8015824T>C , CM000679.2:g.8015824T>C | GRCh38 |
| NC_000017.10:g.7919142T>C , CM000679.1:g.7919142T>C | GRCh37 |
| NC_000017.9:g.7859867T>C | NCBI36 |
| NG_009092.1:g.18155T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254854.5:c.3026T>C MANE Select | ENSP00000254854.4:p.Met1009Thr | |
| ENST00000254854.4:c.3026T>C | ENSP00000254854.4:p.Met1009Thr | |
| NM_000180.3:c.3026T>C | NP_000171.1:p.Met1009Thr | |
| XM_011523816.1:c.3026T>C | XP_011522118.1:p.Met1009Thr | |
| NM_000180.4:c.3026T>C MANE Select | NP_000171.1:p.Met1009Thr |