Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48360053C>G , CM000675.2:g.48360053C>G | GRCh38 |
| NC_000013.10:g.48934189C>G , CM000675.1:g.48934189C>G | GRCh37 |
| NC_000013.9:g.47832190C>G | NCBI36 |
| NG_009009.1:g.61307C>G , LRG_517:g.61307C>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000321.3:c.644C>G MANE Select | NP_000312.2:p.Ser215Ter |
| ENST00000267163.6:c.644C>G MANE Select | ENSP00000267163.4:p.Ser215Ter |
| NM_000321.2:c.644C>G , LRG_517t1:c.644C>G | NP_000312.2:p.Ser215Ter |
| ENST00000267163.4:c.644C>G | ENSP00000267163.4:p.Ser215Ter |
| ENST00000467505.5:c.*12C>G | ENSP00000434702.1:n.*12C>G |
| ENST00000525036.1:n.806C>G | |
| ENST00000650461.1:c.644C>G | ENSP00000497193.1:p.Ser215Ter |
| XM_011535171.1:c.383C>G | XP_011533473.1:p.Ser128Ter |
| XM_011535171.2:c.383C>G | XP_011533473.1:p.Ser128Ter |