Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154861762C>T , CM000685.2:g.154861762C>T | GRCh38 |
| NC_000023.10:g.154090037C>T , CM000685.1:g.154090037C>T | GRCh37 |
| NC_000023.9:g.153743231C>T | NCBI36 |
| NG_011403.1:g.165962G>A | |
| NG_011403.2:g.165962G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000132.4:c.6679G>A MANE Select | NP_000123.1:p.Ala2227Thr |
| ENST00000360256.9:c.6679G>A MANE Select | ENSP00000353393.4:p.Ala2227Thr |
| NM_000132.3:c.6679G>A | NP_000123.1:p.Ala2227Thr |
| NM_019863.2:c.274G>A | NP_063916.1:p.Ala92Thr |
| NM_019863.3:c.274G>A | NP_063916.1:p.Ala92Thr |
| ENST00000330287.10:c.274G>A | ENSP00000327895.6:p.Ala92Thr |
| ENST00000360256.8:c.6679G>A | ENSP00000353393.4:p.Ala2227Thr |
| ENST00000644698.1:c.412G>A | ENSP00000495706.1:p.Ala138Thr |
| XM_011531126.1:c.6574G>A | XP_011529428.1:p.Ala2192Thr |