HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21176828A>G , CM000674.2:g.21176828A>G | GRCh38 |
NC_000012.11:g.21329762A>G , CM000674.1:g.21329762A>G | GRCh37 |
NC_000012.10:g.21221029A>G | NCBI36 |
NG_011745.1:g.50635A>G , LRG_1022:g.50635A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000256958.3:c.412A>G MANE Select | ENSP00000256958.2:p.Thr138Ala | |
ENST00000256958.2:c.412A>G | ENSP00000256958.2:p.Thr138Ala | |
ENST00000543498.5:c.478A>G | ||
NM_006446.4:c.412A>G , LRG_1022t1:c.412A>G | NP_006437.3:p.Thr138Ala | |
NM_006446.5:c.412A>G MANE Select | NP_006437.3:p.Thr138Ala |