Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.141973455T>C , CM000669.2:g.141973455T>C | GRCh38 |
| NC_000007.13:g.141673255T>C , CM000669.1:g.141673255T>C | GRCh37 |
| NC_000007.12:g.141319724T>C | NCBI36 |
| NG_016141.1:g.5319A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_176817.5:c.235A>G (TAS2R38) MANE Select | NP_789787.5:p.Thr79Ala |
| ENST00000547270.1:c.235A>G (TAS2R38) MANE Select | ENSP00000448219.1:p.Thr79Ala |
| NM_176817.4:c.235A>G (TAS2R38) | NP_789787.4:p.Thr79Ala |
| ENST00000465654.5:c.-3+27458T>C (MGAM) | ENSP00000419372.1:n.-3+27458T>C |
| XM_011515783.1:c.*25-12941T>C (OR9A4) | XP_011514085.1:n.*25-12941T>C |