Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.120633301A>G , CM000665.2:g.120633301A>G | GRCh38 |
| NC_000003.11:g.120352148A>G , CM000665.1:g.120352148A>G | GRCh37 |
| NC_000003.10:g.121834838A>G | NCBI36 |
| NG_011957.1:g.54181T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000187.4:c.1034T>C MANE Select | NP_000178.2:p.Leu345Pro |
| ENST00000283871.10:c.1034T>C MANE Select | ENSP00000283871.5:p.Leu345Pro |
| NM_000187.3:c.1034T>C | NP_000178.2:p.Leu345Pro |
| ENST00000283871.9:c.1034T>C | ENSP00000283871.5:p.Leu345Pro |
| ENST00000470321.1:n.374T>C | |
| ENST00000492108.5:c.313T>C | ENSP00000419838.1:n.313T>C |
| XM_005247412.1:c.809T>C | XP_005247469.1:p.Leu270Pro |
| XM_005247412.2:c.809T>C | XP_005247469.1:p.Leu270Pro |
| XM_017006277.2:c.611T>C | XP_016861766.1:p.Leu204Pro |