Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.111098333A>C , CM000667.2:g.111098333A>C | GRCh38 |
| NC_000005.9:g.110434031A>C , CM000667.1:g.110434031A>C | GRCh37 |
| NC_000005.8:g.110461930A>C | NCBI36 |
| NG_008979.1:g.11162A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000513710.4:c.292-389A>C MANE Select | ENSP00000424628.3:n.292-389A>C | |
| ENST00000504122.2:n.174-389A>C | ||
| ENST00000505303.5:n.428-389A>C | ||
| ENST00000506538.6:c.460-389A>C | ENSP00000423067.2:n.460-389A>C | |
| ENST00000513710.3:c.292-389A>C | ENSP00000424628.3:n.292-389A>C | |
| ENST00000612402.4:c.460-389A>C | ENSP00000479950.1:n.460-389A>C | |
| NM_139281.2:c.460-389A>C | NP_644810.1:n.460-389A>C | |
| XM_011543163.1:c.460-389A>C | XP_011541465.1:n.460-389A>C | |
| NM_139281.3:c.292-389A>C MANE Select | NP_644810.2:n.292-389A>C |