HGVS | Genome Assembly |
---|---|
NC_000022.11:g.27750955A>G , CM000684.2:g.27750955A>G | GRCh38 |
NC_000022.10:g.28146943A>G , CM000684.1:g.28146943A>G | GRCh37 |
NC_000022.9:g.26476943A>G | NCBI36 |
NG_023258.1:g.55544T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000703102.1:n.448T>C | ||
ENST00000302326.5:c.3923T>C MANE Select | ENSP00000304956.4:p.Ile1308Thr | |
ENST00000302326.4:c.3923T>C | ENSP00000304956.4:p.Ile1308Thr | |
ENST00000424656.1:c.276T>C | ||
ENST00000497225.1:n.279T>C | ||
NM_002430.2:c.3923T>C | NP_002421.3:p.Ile1308Thr | |
NM_002430.3:c.3923T>C MANE Select | NP_002421.3:p.Ile1308Thr |