Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.46853725C>G , CM000685.2:g.46853725C>G | GRCh38 |
| NC_000023.10:g.46713160C>G , CM000685.1:g.46713160C>G | GRCh37 |
| NC_000023.9:g.46598104C>G | NCBI36 |
| NG_009107.1:g.21814C>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006915.3:c.352C>G MANE Select | NP_008846.2:p.Arg118Gly |
| ENST00000218340.4:c.352C>G MANE Select | ENSP00000218340.3:p.Arg118Gly |
| NM_006915.2:c.352C>G | NP_008846.2:p.Arg118Gly |
| ENST00000218340.3:c.352C>G | ENSP00000218340.3:p.Arg118Gly |