Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94780508G>C , CM000672.2:g.94780508G>C | GRCh38 |
| NC_000010.10:g.96540265G>C , CM000672.1:g.96540265G>C | GRCh37 |
| NC_000010.9:g.96530255G>C | NCBI36 |
| NG_008384.2:g.22803G>C | |
| NG_008384.3:g.22828G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000769.4:c.491G>C MANE Select | NP_000760.1:p.Cys164Ser |
| ENST00000371321.9:c.491G>C MANE Select | ENSP00000360372.3:p.Cys164Ser |
| NM_000769.2:c.491G>C | NP_000760.1:p.Cys164Ser |
| ENST00000371321.7:c.491G>C | ENSP00000360372.3:p.Cys164Ser |
| ENST00000464755.1:c.1254G>C | ENSP00000483243.1:n.1254G>C |
| ENST00000645461.1:n.1544G>C |