HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154997045T>C , CM000685.2:g.154997045T>C | GRCh38 |
NC_000023.10:g.154225320T>C , CM000685.1:g.154225320T>C | GRCh37 |
NC_000023.9:g.153878514T>C | NCBI36 |
NG_011403.1:g.30679A>G | |
NG_011403.2:g.30679A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000360256.9:c.316A>G MANE Select | ENSP00000353393.4:p.Thr106Ala | |
ENST00000647125.1:c.*102A>G | ENSP00000496062.1:n.*102A>G | |
ENST00000360256.8:c.316A>G | ENSP00000353393.4:p.Thr106Ala | |
ENST00000423959.5:c.211A>G | ENSP00000409446.1:p.Thr71Ala | |
ENST00000453950.1:c.298A>G | ENSP00000389153.1:p.Thr100Ala | |
NM_000132.3:c.316A>G | NP_000123.1:p.Thr106Ala | |
XM_011531126.1:c.211A>G | XP_011529428.1:p.Thr71Ala | |
NM_000132.4:c.316A>G MANE Select | NP_000123.1:p.Thr106Ala |