Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.114677631T>G , CM000674.2:g.114677631T>G | GRCh38 |
| NC_000012.11:g.115115436T>G , CM000674.1:g.115115436T>G | GRCh37 |
| NC_000012.10:g.113599819T>G | NCBI36 |
| NG_008315.1:g.11534A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000349155.7:c.830A>C MANE Select | ENSP00000257567.2:p.Asn277Thr | |
| ENST00000257566.7:c.890A>C | ENSP00000257566.3:p.Asn297Thr | |
| ENST00000349155.6:c.830A>C | ENSP00000257567.2:p.Asn277Thr | |
| ENST00000548503.1:n.455A>C | ||
| ENST00000613550.1:c.830A>C | ENSP00000480048.1:p.Asn277Thr | |
| NM_005996.3:c.830A>C | NP_005987.3:p.Asn277Thr | |
| NM_016569.3:c.890A>C | NP_057653.3:p.Asn297Thr | |
| NM_005996.4:c.830A>C MANE Select | NP_005987.3:p.Asn277Thr | |
| NM_016569.4:c.890A>C | NP_057653.3:p.Asn297Thr |