Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.3225637A>G , CM000668.2:g.3225637A>G | GRCh38 |
| NC_000006.11:g.3225871A>G , CM000668.1:g.3225871A>G | GRCh37 |
| NC_000006.10:g.3170870A>G | NCBI36 |
| NG_016715.1:g.7098T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000259818.8:c.452T>C MANE Select | ENSP00000259818.6:p.Leu151Pro | |
| ENST00000680070.1:n.1382T>C | ||
| ENST00000681707.1:n.1279T>C | ||
| ENST00000681757.1:n.757T>C | ||
| ENST00000259818.7:c.452T>C | ENSP00000259818.6:p.Leu151Pro | |
| ENST00000473006.1:n.569T>C | ||
| NM_178012.4:c.452T>C | NP_821080.1:p.Leu151Pro | |
| XM_011514571.1:c.236T>C | XP_011512873.1:p.Leu79Pro | |
| NM_178012.5:c.452T>C MANE Select | NP_821080.1:p.Leu151Pro |