Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10650325C>G , CM000682.2:g.10650325C>G | GRCh38 |
| NC_000020.10:g.10630973C>G , CM000682.1:g.10630973C>G | GRCh37 |
| NC_000020.9:g.10578973C>G | NCBI36 |
| NG_007496.1:g.28722G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000214.3:c.1156G>C MANE Select | NP_000205.1:p.Gly386Arg |
| ENST00000254958.10:c.1156G>C MANE Select | ENSP00000254958.4:p.Gly386Arg |
| NM_000214.2:c.1156G>C | NP_000205.1:p.Gly386Arg |
| ENST00000254958.9:c.1156G>C | ENSP00000254958.4:p.Gly386Arg |
| ENST00000423891.6:n.1022G>C | |
| ENST00000617965.2:n.1745G>C |