MyVariant.info:
GRCh38
chr9:g.133428750G>C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133428750G>C , CM000671.2:g.133428750G>C | GRCh38 |
| NC_000009.10:g.135283691G>C | NCBI36 |
| NG_011934.2:g.19412G>C , LRG_544:g.19412G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355699.7:c.803G>C MANE Select | ENSP00000347927.2:p.Arg268Pro | |
| ENST00000355699.6:c.803G>C | ENSP00000347927.2:p.Arg268Pro | |
| ENST00000356589.6:c.803G>C | ENSP00000348997.2:p.Arg268Pro | |
| ENST00000371911.7:c.803G>C | ENSP00000360979.3:p.Arg268Pro | |
| ENST00000371916.5:c.59G>C | ENSP00000360984.2:p.Arg20Pro | |
| ENST00000371929.7:c.803G>C | ENSP00000360997.3:p.Arg268Pro | |
| ENST00000474918.1:c.686+2405G>C | ENSP00000435305.1:n.686+2405G>C | |
| ENST00000485925.5:n.868+2405G>C | ||
| ENST00000495234.5:c.803G>C | ENSP00000435274.1:p.Arg268Pro | |
| NM_139025.4:c.803G>C , LRG_544t1:c.803G>C | NP_620594.1:p.Arg268Pro | |
| NM_139026.4:c.803G>C | NP_620595.1:p.Arg268Pro | |
| NM_139027.4:c.803G>C | NP_620596.2:p.Arg268Pro | |
| NR_024514.2:n.887+2405G>C | ||
| XM_011518174.1:c.413G>C | XP_011516476.1:p.Arg138Pro | |
| XM_011518175.1:c.803G>C | XP_011516477.1:p.Arg268Pro | |
| XM_011518177.1:c.-4+2405G>C | XP_011516479.1:n.-4+2405G>C | |
| XM_011518180.1:c.686+2405G>C | XP_011516482.1:n.686+2405G>C | |
| XM_017014232.1:c.791G>C | XP_016869721.1:p.Arg264Pro | |
| XM_017014233.1:c.413G>C | XP_016869722.1:p.Arg138Pro | |
| XM_017014234.2:c.-4+2405G>C | XP_016869723.1:n.-4+2405G>C | |
| XM_017014235.1:c.803G>C | XP_016869724.1:p.Arg268Pro | |
| XR_001746171.1:n.2028G>C | ||
| NM_139026.5:c.803G>C | NP_620595.1:p.Arg268Pro | |
| NM_139027.5:c.803G>C | NP_620596.2:p.Arg268Pro | |
| NM_139025.5:c.803G>C | NP_620594.1:p.Arg268Pro | |
| NM_139026.6:c.803G>C | NP_620595.1:p.Arg268Pro | |
| NM_139027.6:c.803G>C MANE Select | NP_620596.2:p.Arg268Pro | |
| NR_024514.3:n.889+2405G>C |