HGVS | Genome Assembly |
---|---|
NC_000001.11:g.186673772T>G , CM000663.2:g.186673772T>G | GRCh38 |
NC_000001.10:g.186642904T>G , CM000663.1:g.186642904T>G | GRCh37 |
NC_000001.9:g.184909527T>G | NCBI36 |
NG_028206.2:g.11656A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367468.10:c.*581A>C MANE Select | ENSP00000356438.5:n.*581A>C | |
ENST00000680451.1:c.*581A>C | ENSP00000506242.1:n.*581A>C | |
ENST00000681605.1:c.*2068A>C | ENSP00000504900.1:n.*2068A>C | |
ENST00000367468.9:c.*581A>C | ENSP00000356438.5:n.*581A>C | |
ENST00000490885.6:n.2811A>C | ||
NM_000963.3:c.*581A>C | NP_000954.1:n.*581A>C | |
NM_000963.4:c.*581A>C MANE Select | NP_000954.1:n.*581A>C |