HGVS | Genome Assembly |
---|---|
NC_000014.9:g.93218706G>A , CM000676.2:g.93218706G>A | GRCh38 |
NC_000014.8:g.93685052G>A , CM000676.1:g.93685052G>A | GRCh37 |
NC_000014.7:g.92754805G>A | NCBI36 |
NG_051089.1:g.16651G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000013070.11:c.781G>A MANE Select | ENSP00000013070.6:p.Ala261Thr | |
ENST00000013070.10:c.781G>A | ENSP00000013070.6:p.Ala261Thr | |
ENST00000416753.5:c.553G>A | ENSP00000391706.2:p.Ala185Thr | |
ENST00000553674.1:c.*482G>A | ENSP00000450470.1:n.*482G>A | |
ENST00000553857.5:c.378+3425G>A | ||
ENST00000555329.1:c.26G>A | ||
NM_175748.3:c.781G>A | NP_786924.2:p.Ala261Thr | |
NR_038150.1:n.883G>A | ||
NM_175748.4:c.781G>A MANE Select | NP_786924.2:p.Ala261Thr | |
NR_038150.2:n.683G>A |