Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48459786A>G , CM000675.2:g.48459786A>G | GRCh38 |
| NC_000013.10:g.49033922A>G , CM000675.1:g.49033922A>G | GRCh37 |
| NC_000013.9:g.47931923A>G | NCBI36 |
| NG_009009.1:g.161040A>G , LRG_517:g.161040A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000267163.6:c.2059A>G MANE Select | ENSP00000267163.4:p.Thr687Ala | |
| ENST00000643064.1:c.194+78343A>G | ||
| ENST00000650461.1:c.2059A>G | ENSP00000497193.1:p.Thr687Ala | |
| ENST00000267163.4:c.2059A>G | ENSP00000267163.4:p.Thr687Ala | |
| NM_000321.2:c.2059A>G , LRG_517t1:c.2059A>G | NP_000312.2:p.Thr687Ala | |
| XM_011535171.1:c.1798A>G | XP_011533473.1:p.Thr600Ala | |
| XM_011535171.2:c.1798A>G | XP_011533473.1:p.Thr600Ala | |
| NM_000321.3:c.2059A>G MANE Select | NP_000312.2:p.Thr687Ala |