Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.143485201G>C , CM000668.2:g.143485201G>C | GRCh38 |
| NC_000006.11:g.143806338G>C , CM000668.1:g.143806338G>C | GRCh37 |
| NC_000006.10:g.143848031G>C | NCBI36 |
| NG_008459.1:g.39421G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003630.3:c.991G>C MANE Select | NP_003621.1:p.Gly331Arg |
| ENST00000367591.5:c.991G>C MANE Select | ENSP00000356563.4:p.Gly331Arg |
| NM_003630.2:c.991G>C | NP_003621.1:p.Gly331Arg |
| ENST00000367591.4:c.991G>C | ENSP00000356563.4:p.Gly331Arg |
| ENST00000585848.1:n.130G>C |