Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.117837142C>G , CM000670.2:g.117837142C>G | GRCh38 |
| NC_000008.10:g.118849381C>G , CM000670.1:g.118849381C>G | GRCh37 |
| NC_000008.9:g.118918562C>G | NCBI36 |
| NG_007455.2:g.279678G>C , LRG_493:g.279678G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684189.1:n.489G>C | ||
| ENST00000378204.7:c.1022G>C MANE Select | ENSP00000367446.3:p.Arg341Thr | |
| ENST00000436216.2:c.390G>C | ||
| ENST00000378204.6:c.1022G>C | ENSP00000367446.2:p.Arg341Thr | |
| ENST00000436216.1:c.390G>C | ||
| ENST00000437196.1:c.74-1591G>C | ENSP00000407299.1:n.74-1591G>C | |
| NM_000127.2:c.1022G>C , LRG_493t1:c.1022G>C | NP_000118.2:p.Arg341Thr | |
| NM_000127.3:c.1022G>C MANE Select | NP_000118.2:p.Arg341Thr |