Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.35752643T>C , CM000679.2:g.35752643T>C | GRCh38 |
| NC_000017.10:g.34079662T>C , CM000679.1:g.34079662T>C | GRCh37 |
| NC_000017.9:g.31103775T>C | NCBI36 |
| NG_029638.1:g.5236A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_139285.4:c.208A>G (GAS2L2) MANE Select | NP_644814.1:p.Asn70Asp |
| ENST00000604641.6:c.208A>G (GAS2L2) MANE Select | ENSP00000474529.2:p.Asn70Asp |
| NM_139285.3:c.208A>G (GAS2L2) | NP_644814.1:p.Asn70Asp |
| ENST00000603067.5:n.6+38847T>C (TAF15) | |
| ENST00000604063.5:c.208A>G (GAS2L2) | ENSP00000474009.1:p.Asn70Asp |
| ENST00000604641.5:c.208A>G (GAS2L2) | ENSP00000474529.1:p.Asn70Asp |
| ENST00000618498.1:c.208A>G (GAS2L2) | ENSP00000480457.1:p.Asn70Asp |
| XM_006721796.2:c.208A>G (GAS2L2) | XP_006721859.1:p.Asn70Asp |