Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.35753046C>A , CM000679.2:g.35753046C>A | GRCh38 |
| NC_000017.10:g.34080065C>A , CM000679.1:g.34080065C>A | GRCh37 |
| NC_000017.9:g.31104178C>A | NCBI36 |
| NG_029638.1:g.4833G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_139285.4:c.-196G>T (GAS2L2) MANE Select | NP_644814.1:n.-196G>T |
| ENST00000604641.6:c.-196G>T (GAS2L2) MANE Select | ENSP00000474529.2:n.-196G>T |
| ENST00000603067.5:n.6+39250C>A (TAF15) | |
| XM_006721796.2:c.-196G>T (GAS2L2) | XP_006721859.1:n.-196G>T |