Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.118168087T>C , CM000673.2:g.118168087T>C | GRCh38 |
| NC_000011.9:g.118038802T>C , CM000673.1:g.118038802T>C | GRCh37 |
| NC_000011.8:g.117544012T>C | NCBI36 |
| NG_042217.1:g.13536A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000278947.6:c.446A>G MANE Select | ENSP00000278947.5:p.Glu149Gly | |
| ENST00000658882.1:c.*271A>G | ENSP00000499572.1:n.*271A>G | |
| ENST00000669850.1:n.688A>G | ||
| ENST00000278947.5:c.446A>G | ENSP00000278947.5:p.Glu149Gly | |
| NM_004588.4:c.446A>G | NP_004579.1:p.Glu149Gly | |
| NM_004588.5:c.446A>G MANE Select | NP_004579.1:p.Glu149Gly |