HGVS | Genome Assembly |
---|---|
NC_000012.12:g.66228282C>T , CM000674.2:g.66228282C>T | GRCh38 |
NC_000012.11:g.66622062C>T , CM000674.1:g.66622062C>T | GRCh37 |
NC_000012.10:g.64908329C>T | NCBI36 |
NG_021194.1:g.44085C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261233.9:c.799C>T MANE Select | ENSP00000261233.4:p.Arg267Ter | |
ENST00000261233.8:c.799C>T | ENSP00000261233.4:p.Arg267Ter | |
ENST00000457197.2:c.616C>T | ENSP00000409852.2:p.Arg206Ter | |
NM_001142523.1:c.616C>T | NP_001135995.1:p.Arg206Ter | |
NM_007199.2:c.799C>T | NP_009130.2:p.Arg267Ter | |
NM_001142523.2:c.616C>T | NP_001135995.1:p.Arg206Ter | |
NM_007199.3:c.799C>T MANE Select | NP_009130.2:p.Arg267Ter |