Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32440944T>C , CM000668.2:g.32440944T>C | GRCh38 |
| NC_000006.11:g.32408721T>C , CM000668.1:g.32408721T>C | GRCh37 |
| NC_000006.10:g.32516699T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395388.7:c.82+912T>C MANE Select | ENSP00000378786.2:n.82+912T>C | |
| ENST00000374982.5:c.82+912T>C | ENSP00000364121.5:n.82+912T>C | |
| ENST00000395388.6:c.82+912T>C | ENSP00000378786.2:n.82+912T>C | |
| NM_019111.4:c.82+912T>C | NP_061984.2:n.82+912T>C | |
| NM_019111.5:c.82+912T>C MANE Select | NP_061984.2:n.82+912T>C |