Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.117812920T>C , CM000670.2:g.117812920T>C | GRCh38 |
| NC_000008.10:g.118825159T>C , CM000670.1:g.118825159T>C | GRCh37 |
| NC_000008.9:g.118894340T>C | NCBI36 |
| NG_007455.2:g.303900A>G , LRG_493:g.303900A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000127.3:c.1674A>G MANE Select | NP_000118.2:p.Thr558= |
| ENST00000378204.7:c.1674A>G MANE Select | ENSP00000367446.3:p.Thr558= |
| NM_000127.2:c.1674A>G , LRG_493t1:c.1674A>G | NP_000118.2:p.Thr558= |
| ENST00000378204.6:c.1674A>G | ENSP00000367446.2:p.Thr558= |
| ENST00000437196.1:c.*565A>G | ENSP00000407299.1:n.*565A>G |
| ENST00000684189.1:n.1141A>G |