Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.23867918G>A , CM000663.2:g.23867918G>A | GRCh38 |
| NC_000001.10:g.24194408G>A , CM000663.1:g.24194408G>A | GRCh37 |
| NC_000001.9:g.24066995G>A | NCBI36 |
| NG_013346.1:g.5452C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374479.4:c.369C>T MANE Select | ENSP00000363603.3:p.Leu123= | |
| ENST00000374479.3:c.369C>T | ENSP00000363603.3:p.Leu123= | |
| NM_000147.4:c.369C>T | NP_000138.2:p.Leu123= | |
| XM_005245821.1:c.-181C>T | XP_005245878.1:n.-181C>T | |
| XM_005245821.3:c.-181C>T | XP_005245878.1:n.-181C>T | |
| NM_000147.5:c.369C>T MANE Select | NP_000138.2:p.Leu123= | |
| NR_174379.1:n.373C>T | ||
| NR_174380.1:n.373C>T | ||
| NR_174381.1:n.373C>T | ||
| NR_174382.1:n.373C>T |