Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48342673G>T , CM000675.2:g.48342673G>T | GRCh38 |
| NC_000013.10:g.48916809G>T , CM000675.1:g.48916809G>T | GRCh37 |
| NC_000013.9:g.47814810G>T | NCBI36 |
| NG_009009.1:g.43927G>T , LRG_517:g.43927G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000321.3:c.339G>T MANE Select | NP_000312.2:p.Met113Ile |
| ENST00000267163.6:c.339G>T MANE Select | ENSP00000267163.4:p.Met113Ile |
| NM_000321.2:c.339G>T , LRG_517t1:c.339G>T | NP_000312.2:p.Met113Ile |
| ENST00000267163.4:c.339G>T | ENSP00000267163.4:p.Met113Ile |
| ENST00000467505.5:c.138-17344G>T | ENSP00000434702.1:n.138-17344G>T |
| ENST00000525036.1:n.501G>T | |
| ENST00000650461.1:c.339G>T | ENSP00000497193.1:p.Met113Ile |
| XM_011535171.1:c.78G>T | XP_011533473.1:p.Met26Ile |
| XM_011535171.2:c.78G>T | XP_011533473.1:p.Met26Ile |