HGVS | Genome Assembly |
---|---|
NC_000023.11:g.136659416A= , CM000685.2:g.136659416A= | GRCh38 |
NC_000023.10:g.135741575A= , CM000685.1:g.135741575A= | GRCh37 |
NC_000023.9:g.135569241A= | NCBI36 |
NG_007280.1:g.16240A= , LRG_141:g.16240A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000695724.1:c.*405A= | ENSP00000512122.1:n.*405A= | |
ENST00000695725.1:c.*342A= | ENSP00000512123.1:n.*342A= | |
ENST00000695726.1:n.2755A= | ||
ENST00000695729.1:n.3590A= | ||
ENST00000370629.7:c.*1A= MANE Select | ENSP00000359663.2:n.*1A= | |
ENST00000370628.2:c.*1A= | ENSP00000359662.2:n.*1A= | |
ENST00000370629.6:c.*1A= | ENSP00000359663.2:n.*1A= | |
NM_000074.2:c.*1A= , LRG_141t1:c.*1A= | NP_000065.1:n.*1A= | |
NM_000074.3:c.*1A= MANE Select | NP_000065.1:n.*1A= |