Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6713280C>G , CM000681.2:g.6713280C>G | GRCh38 |
| NC_000019.9:g.6713291C>G , CM000681.1:g.6713291C>G | GRCh37 |
| NC_000019.8:g.6664291C>G | NCBI36 |
| NG_009557.1:g.12372G>C , LRG_27:g.12372G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000064.4:c.912G>C MANE Select | NP_000055.2:p.Arg304= |
| ENST00000245907.11:c.912G>C MANE Select | ENSP00000245907.4:p.Arg304= |
| NM_000064.3:c.912G>C | NP_000055.2:p.Arg304= |
| ENST00000245907.10:c.912G>C | ENSP00000245907.4:p.Arg304= |
| ENST00000594270.5:n.36G>C | |
| ENST00000595577.1:n.416G>C | |
| ENST00000597442.5:n.162G>C | |
| ENST00000695652.1:c.789G>C | ENSP00000512083.1:p.Arg263= |
| ENST00000695654.1:c.36G>C | ENSP00000512085.1:p.Arg12= |
| ENST00000695692.1:n.236G>C |