HGVS | Genome Assembly |
---|---|
NC_000014.9:g.91273445C>G , CM000676.2:g.91273445C>G | GRCh38 |
NC_000014.8:g.91739789C>G , CM000676.1:g.91739789C>G | GRCh37 |
NC_000014.7:g.90809542C>G | NCBI36 |
NG_033118.1:g.149400G>C | |
NG_033118.2:g.149400G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000389857.11:c.5267G>C MANE Select | ENSP00000374507.6:p.Arg1756Thr | |
ENST00000331194.8:c.839G>C | ENSP00000330332.8:p.Arg280Thr | |
ENST00000389857.10:c.5267G>C | ENSP00000374507.6:p.Arg1756Thr | |
ENST00000556726.5:c.1495G>C | ||
NM_001080414.3:c.5267G>C | NP_001073883.2:p.Arg1756Thr | |
XM_011536796.1:c.5159G>C | XP_011535098.1:p.Arg1720Thr | |
XM_011536796.2:c.5159G>C | XP_011535098.1:p.Arg1720Thr | |
XM_017021336.1:c.2348G>C | XP_016876825.1:p.Arg783Thr | |
NM_001080414.4:c.5267G>C MANE Select | NP_001073883.2:p.Arg1756Thr |