Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19961067G>C , CM000670.2:g.19961067G>C | GRCh38 |
| NC_000008.10:g.19818578G>C , CM000670.1:g.19818578G>C | GRCh37 |
| NC_000008.9:g.19862858G>C | NCBI36 |
| NG_008855.1:g.26997G>C | |
| NG_008855.2:g.64351G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000237.3:c.1306G>C MANE Select | NP_000228.1:p.Gly436Arg |
| ENST00000650287.1:c.1306G>C MANE Select | ENSP00000497642.1:p.Gly436Arg |
| NM_000237.2:c.1306G>C | NP_000228.1:p.Gly436Arg |
| ENST00000311322.8:c.1306G>C | ENSP00000309757.6:p.Gly436Arg |
| ENST00000650478.1:c.246G>C | ENSP00000497560.1:n.246G>C |