Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.176711575G>A , CM000666.2:g.176711575G>A | GRCh38 |
| NC_000004.11:g.177632729G>A , CM000666.1:g.177632729G>A | GRCh37 |
| NC_000004.10:g.177869723G>A | NCBI36 |
| NG_034216.1:g.86171C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000618562.2:c.628C>T MANE Select | ENSP00000480043.1:p.Arg210Ter | |
| ENST00000507638.1:n.327C>T | ||
| ENST00000618562.1:c.628C>T | ENSP00000480043.1:p.Arg210Ter | |
| NM_005429.4:c.628C>T | NP_005420.1:p.Arg210Ter | |
| NM_005429.5:c.628C>T MANE Select | NP_005420.1:p.Arg210Ter |