Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.18121732G>C , CM000668.2:g.18121732G>C | GRCh38 |
| NC_000006.11:g.18121963G>C , CM000668.1:g.18121963G>C | GRCh37 |
| NC_000006.10:g.18229942G>C | NCBI36 |
| NG_016750.1:g.5889C>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_198586.3:c.875C>G MANE Select | NP_940988.2:p.Thr292Ser |
| ENST00000340650.6:c.875C>G MANE Select | ENSP00000345464.3:p.Thr292Ser |
| NM_198586.2:c.875C>G | NP_940988.2:p.Thr292Ser |
| ENST00000340650.4:c.875C>G | ENSP00000345464.3:p.Thr292Ser |