Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48349005A>G , CM000675.2:g.48349005A>G | GRCh38 |
| NC_000013.10:g.48923141A>G , CM000675.1:g.48923141A>G | GRCh37 |
| NC_000013.9:g.47821142A>G | NCBI36 |
| NG_009009.1:g.50259A>G , LRG_517:g.50259A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000267163.6:c.589A>G MANE Select | ENSP00000267163.4:p.Thr197Ala | |
| ENST00000650461.1:c.589A>G | ENSP00000497193.1:p.Thr197Ala | |
| ENST00000267163.4:c.589A>G | ENSP00000267163.4:p.Thr197Ala | |
| ENST00000467505.5:c.138-11012A>G | ENSP00000434702.1:n.138-11012A>G | |
| ENST00000525036.1:n.751A>G | ||
| NM_000321.2:c.589A>G , LRG_517t1:c.589A>G | NP_000312.2:p.Thr197Ala | |
| XM_011535171.1:c.328A>G | XP_011533473.1:p.Thr110Ala | |
| XM_011535171.2:c.328A>G | XP_011533473.1:p.Thr110Ala | |
| NM_000321.3:c.589A>G MANE Select | NP_000312.2:p.Thr197Ala |