Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.66346230A>G , CM000673.2:g.66346230A>G | GRCh38 |
| NC_000011.9:g.66113701A>G , CM000673.1:g.66113701A>G | GRCh37 |
| NC_000011.8:g.65870277A>G | NCBI36 |
| NG_033202.1:g.6461T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006876.3:c.1067T>C MANE Select | NP_006867.1:p.Leu356Pro |
| ENST00000311181.5:c.1067T>C MANE Select | ENSP00000309096.4:p.Leu356Pro |
| NM_006876.2:c.1067T>C | NP_006867.1:p.Leu356Pro |
| ENST00000311181.4:c.1067T>C | ENSP00000309096.4:p.Leu356Pro |