HGVS | Genome Assembly |
---|---|
NC_000007.14:g.141972806G>T , CM000669.2:g.141972806G>T | GRCh38 |
NC_000007.13:g.141672606G>T , CM000669.1:g.141672606G>T | GRCh37 |
NC_000007.12:g.141319075G>T | NCBI36 |
NG_016141.1:g.5968C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000465654.5:c.-3+26809G>T (MGAM) | ENSP00000419372.1:n.-3+26809G>T | |
ENST00000547270.1:c.884C>A (TAS2R38) MANE Select | ENSP00000448219.1:p.Ala295Asp | |
NM_176817.4:c.884C>A (TAS2R38) | NP_789787.4:p.Ala295Asp | |
XM_011515783.1:c.*25-13590G>T (OR9A4) | XP_011514085.1:n.*25-13590G>T | |
NM_176817.5:c.884C>A (TAS2R38) MANE Select | NP_789787.5:p.Ala295Asp |