Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32202581A>G , CM000668.2:g.32202581A>G | GRCh38 |
| NC_000006.11:g.32170358A>G , CM000668.1:g.32170358A>G | GRCh37 |
| NC_000006.10:g.32278336A>G | NCBI36 |
| NG_028190.1:g.26487T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375023.3:c.3250T>C MANE Select | ENSP00000364163.3:p.Cys1084Arg | |
| ENST00000474612.1:n.1336T>C | ||
| NM_004557.3:c.3250T>C | NP_004548.3:p.Cys1084Arg | |
| NR_134949.1:n.3473-1081T>C | ||
| NR_134950.1:n.3371-1081T>C | ||
| NM_004557.4:c.3250T>C MANE Select | NP_004548.3:p.Cys1084Arg | |
| NR_134949.2:n.3473-1081T>C | ||
| NR_134950.2:n.3371-1081T>C |