Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94417775A>G , CM000669.2:g.94417775A>G | GRCh38 |
| NC_000007.13:g.94047087A>G , CM000669.1:g.94047087A>G | GRCh37 |
| NC_000007.12:g.93885023A>G | NCBI36 |
| NG_007405.1:g.28215A>G , LRG_2:g.28215A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000089.4:c.1915A>G MANE Select | NP_000080.2:p.Ser639Gly |
| ENST00000297268.11:c.1915A>G MANE Select | ENSP00000297268.6:p.Ser639Gly |
| NM_000089.3:c.1915A>G , LRG_2t1:c.1915A>G | NP_000080.2:p.Ser639Gly |
| ENST00000297268.10:c.1915A>G | ENSP00000297268.6:p.Ser639Gly |
| ENST00000461525.5:n.4A>G | |
| ENST00000473573.5:n.252A>G | |
| ENST00000497316.5:n.312A>G | |
| ENST00000620463.1:c.1909A>G | ENSP00000477719.1:p.Ser637Gly |