Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.134498412C>T , CM000685.2:g.134498412C>T | GRCh38 |
| NC_000023.10:g.133632442C>T , CM000685.1:g.133632442C>T | GRCh37 |
| NC_000023.9:g.133460108C>T | NCBI36 |
| NG_012329.1:g.43268C>T | |
| NG_012329.2:g.43268C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000298556.8:c.508C>T MANE Select | ENSP00000298556.7:p.Arg170Ter | |
| ENST00000298556.7:c.508C>T | ENSP00000298556.7:p.Arg170Ter | |
| ENST00000462974.5:n.666C>T | ||
| ENST00000475720.1:n.466C>T | ||
| NM_000194.2:c.508C>T | NP_000185.1:p.Arg170Ter | |
| XM_011531328.1:c.526C>T | XP_011529630.1:p.Arg176Ter | |
| NM_000194.3:c.508C>T MANE Select | NP_000185.1:p.Arg170Ter |