HGVS | Genome Assembly |
---|---|
NC_000016.10:g.84031949C>A , CM000678.2:g.84031949C>A | GRCh38 |
NC_000016.9:g.84065554C>A , CM000678.1:g.84065554C>A | GRCh37 |
NC_000016.8:g.82623055C>A | NCBI36 |
NG_034136.1:g.15209G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000299709.8:c.550G>T MANE Select | ENSP00000299709.3:p.Ala184Ser | |
ENST00000299709.7:c.550G>T | ENSP00000299709.3:p.Ala184Ser | |
ENST00000568178.1:c.550G>T | ENSP00000457737.1:p.Ala184Ser | |
NM_001080442.2:c.550G>T | NP_001073911.1:p.Ala184Ser | |
XM_011522872.1:c.550G>T | XP_011521174.1:p.Ala184Ser | |
XM_017022946.1:c.550G>T | XP_016878435.1:p.Ala184Ser | |
NM_001080442.3:c.550G>T MANE Select | NP_001073911.1:p.Ala184Ser |