Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.91272682G>A , CM000676.2:g.91272682G>A | GRCh38 |
| NC_000014.8:g.91739026G>A , CM000676.1:g.91739026G>A | GRCh37 |
| NC_000014.7:g.90808779G>A | NCBI36 |
| NG_033118.1:g.150163C>T | |
| NG_033118.2:g.150163C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389857.11:c.6030C>T MANE Select | ENSP00000374507.6:p.Ala2010= | |
| ENST00000331194.8:c.1464C>T | ENSP00000330332.8:p.Ala488= | |
| ENST00000389857.10:c.6030C>T | ENSP00000374507.6:p.Ala2010= | |
| ENST00000556726.5:c.2258C>T | ||
| NM_001080414.3:c.6030C>T | NP_001073883.2:p.Ala2010= | |
| XM_011536796.1:c.5922C>T | XP_011535098.1:p.Ala1974= | |
| XM_011536796.2:c.5922C>T | XP_011535098.1:p.Ala1974= | |
| XM_017021336.1:c.3111C>T | XP_016876825.1:p.Ala1037= | |
| NM_001080414.4:c.6030C>T MANE Select | NP_001073883.2:p.Ala2010= |