HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41612391C>T , CM000679.2:g.41612391C>T | GRCh38 |
NC_000017.10:g.39768643C>T , CM000679.1:g.39768643C>T | GRCh37 |
NC_000017.9:g.37022169C>T | NCBI36 |
NG_008301.1:g.5437G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000301653.9:c.298G>A MANE Select | ENSP00000301653.3:p.Ala100Thr | |
ENST00000301653.8:c.298G>A | ENSP00000301653.3:p.Ala100Thr | |
ENST00000588319.1:n.375G>A | ||
ENST00000593067.1:c.-312-105G>A | ENSP00000467124.1:n.-312-105G>A | |
NM_005557.3:c.298G>A | NP_005548.2:p.Ala100Thr | |
NM_005557.4:c.298G>A MANE Select | NP_005548.2:p.Ala100Thr |