Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94408354G>C , CM000669.2:g.94408354G>C | GRCh38 |
| NC_000007.13:g.94037666G>C , CM000669.1:g.94037666G>C | GRCh37 |
| NC_000007.12:g.93875602G>C | NCBI36 |
| NG_007405.1:g.18794G>C , LRG_2:g.18794G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000089.4:c.712G>C MANE Select | NP_000080.2:p.Gly238Arg |
| ENST00000297268.11:c.712G>C MANE Select | ENSP00000297268.6:p.Gly238Arg |
| NM_000089.3:c.712G>C , LRG_2t1:c.712G>C | NP_000080.2:p.Gly238Arg |
| ENST00000297268.10:c.712G>C | ENSP00000297268.6:p.Gly238Arg |
| ENST00000620463.1:c.706G>C | ENSP00000477719.1:p.Gly236Arg |