Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.44942874G>C , CM000664.2:g.44942874G>C | GRCh38 |
| NC_000002.11:g.45170013G>C , CM000664.1:g.45170013G>C | GRCh37 |
| NC_000002.10:g.45023517G>C | NCBI36 |
| NG_016222.1:g.5977G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000260653.5:c.770G>C MANE Select | ENSP00000260653.3:p.Arg257Pro | |
| ENST00000260653.4:c.770G>C | ENSP00000260653.3:p.Arg257Pro | |
| NM_005413.3:c.770G>C | NP_005404.1:p.Arg257Pro | |
| XM_011533042.1:c.770G>C | XP_011531344.1:p.Arg257Pro | |
| NM_005413.4:c.770G>C MANE Select | NP_005404.1:p.Arg257Pro |