HGVS | Genome Assembly |
---|---|
NC_000023.11:g.136659505T>A , CM000685.2:g.136659505T>A | GRCh38 |
NC_000023.10:g.135741664T>A , CM000685.1:g.135741664T>A | GRCh37 |
NC_000023.9:g.135569330T>A | NCBI36 |
NG_007280.1:g.16329T>A , LRG_141:g.16329T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695724.1:c.*494T>A | ENSP00000512122.1:n.*494T>A | |
ENST00000695725.1:c.*431T>A | ENSP00000512123.1:n.*431T>A | |
ENST00000695726.1:n.2844T>A | ||
ENST00000695729.1:n.3679T>A | ||
ENST00000370629.7:c.*90T>A MANE Select | ENSP00000359663.2:n.*90T>A | |
ENST00000370628.2:c.*90T>A | ENSP00000359662.2:n.*90T>A | |
ENST00000370629.6:c.*90T>A | ENSP00000359663.2:n.*90T>A | |
NM_000074.2:c.*90T>A , LRG_141t1:c.*90T>A | NP_000065.1:n.*90T>A | |
NM_000074.3:c.*90T>A MANE Select | NP_000065.1:n.*90T>A |