Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.118110244C>A , CM000670.2:g.118110244C>A | GRCh38 |
| NC_000008.10:g.119122483C>A , CM000670.1:g.119122483C>A | GRCh37 |
| NC_000008.9:g.119191664C>A | NCBI36 |
| NG_007455.2:g.6576G>T , LRG_493:g.6576G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000127.3:c.803G>T MANE Select | NP_000118.2:p.Gly268Val |
| ENST00000378204.7:c.803G>T MANE Select | ENSP00000367446.3:p.Gly268Val |
| NM_000127.2:c.803G>T , LRG_493t1:c.803G>T | NP_000118.2:p.Gly268Val |
| ENST00000378204.6:c.803G>T | ENSP00000367446.2:p.Gly268Val |
| ENST00000436216.1:c.171G>T | |
| ENST00000436216.2:c.171G>T | |
| ENST00000437196.1:c.73+730G>T | ENSP00000407299.1:n.73+730G>T |