HGVS | Genome Assembly |
---|---|
NC_000010.11:g.97598862T>C , CM000672.2:g.97598862T>C | GRCh38 |
NC_000010.10:g.99358619T>C , CM000672.1:g.99358619T>C | GRCh37 |
NC_000010.9:g.99348609T>C | NCBI36 |
NG_027922.1:g.19518T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000370646.9:c.299T>C MANE Select | ENSP00000359680.4:p.Met100Thr | |
ENST00000370646.8:c.299T>C | ENSP00000359680.4:p.Met100Thr | |
ENST00000370647.8:c.212-2995T>C | ENSP00000359681.4:n.212-2995T>C | |
ENST00000370649.3:c.212-2995T>C | ENSP00000359683.3:n.212-2995T>C | |
ENST00000465608.1:n.680T>C | ||
NM_001134670.1:c.212-2995T>C | NP_001128142.1:n.212-2995T>C | |
NM_138413.3:c.299T>C | NP_612422.2:p.Met100Thr | |
NM_138413.4:c.299T>C MANE Select | NP_612422.2:p.Met100Thr | |
NM_001134670.2:c.212-2995T>C | NP_001128142.1:n.212-2995T>C |