Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86632871C>T , CM000670.2:g.86632871C>T | GRCh38 |
| NC_000008.10:g.87645099C>T , CM000670.1:g.87645099C>T | GRCh37 |
| NC_000008.9:g.87714215C>T | NCBI36 |
| NG_016980.1:g.115805G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000320005.6:c.1201G>A MANE Select | ENSP00000316605.5:p.Ala401Thr | |
| ENST00000681546.1:n.1021G>A | ||
| ENST00000681746.1:c.1201G>A | ENSP00000505959.1:p.Ala401Thr | |
| ENST00000320005.5:c.1201G>A | ENSP00000316605.5:p.Ala401Thr | |
| NM_019098.4:c.1201G>A | NP_061971.3:p.Ala401Thr | |
| XM_011517138.1:c.787G>A | XP_011515440.1:p.Ala263Thr | |
| XM_011517138.2:c.787G>A | XP_011515440.1:p.Ala263Thr | |
| NM_019098.5:c.1201G>A MANE Select | NP_061971.3:p.Ala401Thr |