Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.96286829T>C , CM000664.2:g.96286829T>C | GRCh38 |
| NC_000002.11:g.96952567T>C , CM000664.1:g.96952567T>C | GRCh37 |
| NC_000002.10:g.96316294T>C | NCBI36 |
| NG_016973.1:g.23731A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_014014.5:c.3688A>G MANE Select | NP_054733.2:p.Ser1230Gly |
| ENST00000323853.10:c.3688A>G MANE Select | ENSP00000317123.5:p.Ser1230Gly |
| NM_014014.4:c.3688A>G | NP_054733.2:p.Ser1230Gly |
| ENST00000323853.9:c.3688A>G | ENSP00000317123.5:p.Ser1230Gly |
| ENST00000480615.1:n.805A>G | |
| ENST00000652267.1:c.3688A>G | ENSP00000498933.1:p.Ser1230Gly |