HGVS | Genome Assembly |
---|---|
NC_000023.11:g.136648200C= , CM000685.2:g.136648200C= | GRCh38 |
NC_000023.10:g.135730359C= , CM000685.1:g.135730359C= | GRCh37 |
NC_000023.9:g.135558025C= | NCBI36 |
NG_007280.1:g.5024C= , LRG_141:g.5024C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000695724.1:c.-49C= | ENSP00000512122.1:n.-49C= | |
ENST00000695725.1:c.-49C= | ENSP00000512123.1:n.-49C= | |
ENST00000370629.7:c.-49C= MANE Select | ENSP00000359663.2:n.-49C= | |
ENST00000370629.6:c.-49C= | ENSP00000359663.2:n.-49C= | |
NM_000074.2:c.-49C= , LRG_141t1:c.-49C= | NP_000065.1:n.-49C= | |
NM_000074.3:c.-49C= MANE Select | NP_000065.1:n.-49C= |