Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.50130522C>G , CM000676.2:g.50130522C>G | GRCh38 |
| NC_000014.8:g.50597240C>G , CM000676.1:g.50597240C>G | GRCh37 |
| NC_000014.7:g.49666990C>G | NCBI36 |
| NG_051073.1:g.106172G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216373.10:c.3316G>C MANE Select | ENSP00000216373.5:p.Val1106Leu | |
| ENST00000216373.9:c.3316G>C | ENSP00000216373.5:p.Val1106Leu | |
| ENST00000543680.5:c.3217G>C | ENSP00000445328.1:p.Val1073Leu | |
| NM_006939.2:c.3316G>C | NP_008870.2:p.Val1106Leu | |
| XM_005268021.1:c.3136G>C | XP_005268078.1:p.Val1046Leu | |
| XM_011537103.1:c.3277G>C | XP_011535405.1:p.Val1093Leu | |
| NM_006939.3:c.3316G>C | NP_008870.2:p.Val1106Leu | |
| NM_006939.4:c.3316G>C MANE Select | NP_008870.2:p.Val1106Leu |