HGVS | Genome Assembly |
---|---|
NC_000007.14:g.141973341A>C , CM000669.2:g.141973341A>C | GRCh38 |
NC_000007.13:g.141673141A>C , CM000669.1:g.141673141A>C | GRCh37 |
NC_000007.12:g.141319610A>C | NCBI36 |
NG_016141.1:g.5433T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000465654.5:c.-3+27344A>C (MGAM) | ENSP00000419372.1:n.-3+27344A>C | |
ENST00000547270.1:c.349T>G (TAS2R38) MANE Select | ENSP00000448219.1:p.Tyr117Asp | |
NM_176817.4:c.349T>G (TAS2R38) | NP_789787.4:p.Tyr117Asp | |
XM_011515783.1:c.*25-13055A>C (OR9A4) | XP_011514085.1:n.*25-13055A>C | |
NM_176817.5:c.349T>G (TAS2R38) MANE Select | NP_789787.5:p.Tyr117Asp |