Linked Data
gnomAD v4:
14-100882736-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.100882736C>G , CM000676.2:g.100882736C>G | GRCh38 |
| NC_000014.8:g.101349073C>G , CM000676.1:g.101349073C>G | GRCh37 |
| NC_000014.7:g.100418826C>G | NCBI36 |
| NG_045001.1:g.7112G>C | |
| NG_045000.5:g.51468C>G | |
| NG_045000.6:g.51468C>G | |
| NG_045001.2:g.25987G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000649591.1:c.2053G>C MANE Select | ENSP00000497482.1:p.Val685Leu | |
| ENST00000534062.1:c.2053G>C | ENSP00000435342.1:p.Val685Leu | |
| NM_001134888.2:c.2053G>C | NP_001128360.1:p.Val685Leu | |
| NM_001134888.3:c.2053G>C MANE Select | NP_001128360.1:p.Val685Leu |