Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154993083T>G , CM000685.2:g.154993083T>G | GRCh38 |
| NC_000023.10:g.154221358T>G , CM000685.1:g.154221358T>G | GRCh37 |
| NC_000023.9:g.153874552T>G | NCBI36 |
| NG_011403.1:g.34641A>C | |
| NG_011403.2:g.34641A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.454A>C MANE Select | ENSP00000353393.4:p.Ser152Arg | |
| ENST00000647125.1:c.*240A>C | ENSP00000496062.1:n.*240A>C | |
| ENST00000360256.8:c.454A>C | ENSP00000353393.4:p.Ser152Arg | |
| ENST00000423959.5:c.349A>C | ENSP00000409446.1:p.Ser117Arg | |
| ENST00000453950.1:c.436A>C | ENSP00000389153.1:p.Ser146Arg | |
| NM_000132.3:c.454A>C | NP_000123.1:p.Ser152Arg | |
| XM_011531126.1:c.349A>C | XP_011529428.1:p.Ser117Arg | |
| NM_000132.4:c.454A>C MANE Select | NP_000123.1:p.Ser152Arg |