HGVS | Genome Assembly |
---|---|
NC_000023.11:g.136659319A>T , CM000685.2:g.136659319A>T | GRCh38 |
NC_000023.10:g.135741478A>T , CM000685.1:g.135741478A>T | GRCh37 |
NC_000023.9:g.135569144A>T | NCBI36 |
NG_007280.1:g.16143A>T , LRG_141:g.16143A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695724.1:c.*308A>T | ENSP00000512122.1:n.*308A>T | |
ENST00000695725.1:c.*245A>T | ENSP00000512123.1:n.*245A>T | |
ENST00000695726.1:n.2658A>T | ||
ENST00000695729.1:n.3493A>T | ||
ENST00000370629.7:c.690A>T MANE Select | ENSP00000359663.2:p.Glu230Asp | |
ENST00000370628.2:c.627A>T | ENSP00000359662.2:p.Glu209Asp | |
ENST00000370629.6:c.690A>T | ENSP00000359663.2:p.Glu230Asp | |
NM_000074.2:c.690A>T , LRG_141t1:c.690A>T | NP_000065.1:p.Glu230Asp | |
NM_000074.3:c.690A>T MANE Select | NP_000065.1:p.Glu230Asp |