Linked Data
gnomAD v4:
1-115700592-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.115700592C>G , CM000663.2:g.115700592C>G | GRCh38 |
| NC_000001.10:g.116243213C>G , CM000663.1:g.116243213C>G | GRCh37 |
| NC_000001.9:g.116044736C>G | NCBI36 |
| NG_008802.1:g.73214G>C , LRG_404:g.73214G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000488931.2:c.*1221G>C | ENSP00000518226.1:n.*1221G>C | |
| ENST00000261448.6:c.*649G>C MANE Select | ENSP00000261448.5:n.*649G>C | |
| ENST00000261448.5:c.*649G>C | ENSP00000261448.5:n.*649G>C | |
| NM_001232.3:c.*649G>C , LRG_404t1:c.*649G>C | NP_001223.2:n.*649G>C | |
| NM_001232.4:c.*649G>C MANE Select | NP_001223.2:n.*649G>C |