Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.74524387G>C , CM000685.2:g.74524387G>C | GRCh38 |
| NC_000023.10:g.73744222G>C , CM000685.1:g.73744222G>C | GRCh37 |
| NC_000023.9:g.73660947G>C | NCBI36 |
| NG_011641.1:g.108138G>C | |
| NG_011641.2:g.108138G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006517.5:c.604G>C MANE Select | NP_006508.2:p.Gly202Arg |
| ENST00000587091.6:c.604G>C MANE Select | ENSP00000465734.1:p.Gly202Arg |
| NM_006517.4:c.604G>C | NP_006508.2:p.Gly202Arg |
| ENST00000587091.5:c.604G>C | ENSP00000465734.1:p.Gly202Arg |
| ENST00000590447.1:c.44G>C | |
| ENST00000636771.1:c.513G>C | |
| XM_005262294.1:c.604G>C | XP_005262351.1:p.Gly202Arg |
| XM_011531015.1:c.604G>C | XP_011529317.1:p.Gly202Arg |