HGVS | Genome Assembly |
---|---|
NC_000010.11:g.68231594C>G , CM000672.2:g.68231594C>G | GRCh38 |
NC_000010.10:g.69991351C>G , CM000672.1:g.69991351C>G | GRCh37 |
NC_000010.9:g.69661357C>G | NCBI36 |
NG_031934.1:g.5520G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373673.5:c.84G>C MANE Select | ENSP00000362777.3:p.Thr28= | |
ENST00000373673.4:c.84G>C | ENSP00000362777.3:p.Thr28= | |
NM_145178.3:c.84G>C | NP_660161.1:p.Thr28= | |
NM_145178.4:c.84G>C MANE Select | NP_660161.1:p.Thr28= |