HGVS | Genome Assembly |
---|---|
NC_000016.10:g.67436638G>A , CM000678.2:g.67436638G>A | GRCh38 |
NC_000016.9:g.67470541G>A , CM000678.1:g.67470541G>A | GRCh37 |
NC_000016.8:g.66028042G>A | NCBI36 |
NG_011482.1:g.49549C>T | |
NG_016549.1:g.10506G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000326152.6:c.853G>A MANE Select | ENSP00000316786.5:p.Ala285Thr | |
ENST00000326152.5:c.853G>A | ENSP00000316786.5:p.Ala285Thr | |
NM_000196.3:c.853G>A | NP_000187.3:p.Ala285Thr | |
NM_000196.4:c.853G>A MANE Select | NP_000187.3:p.Ala285Thr |