Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.3154780C>G , CM000668.2:g.3154780C>G | GRCh38 |
| NC_000006.11:g.3155014C>G , CM000668.1:g.3155014C>G | GRCh37 |
| NC_000006.10:g.3100013C>G | NCBI36 |
| NG_042223.1:g.7770G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000333628.4:c.421G>C MANE Select | ENSP00000369703.2:p.Gly141Arg | |
| ENST00000679400.1:n.477G>C | ||
| ENST00000679907.1:n.809G>C | ||
| ENST00000680036.1:n.1203G>C | ||
| ENST00000680967.1:n.1511G>C | ||
| ENST00000333628.3:c.421G>C | ENSP00000369703.2:p.Gly141Arg | |
| ENST00000489942.1:n.616G>C | ||
| NM_001069.2:c.421G>C | NP_001060.1:p.Gly141Arg | |
| NM_001310315.1:c.166G>C | NP_001297244.1:p.Gly56Arg | |
| NM_001069.3:c.421G>C MANE Select | NP_001060.1:p.Gly141Arg | |
| NM_001310315.2:c.166G>C | NP_001297244.1:p.Gly56Arg |