HGVS | Genome Assembly |
---|---|
NC_000023.11:g.136648206C= , CM000685.2:g.136648206C= | GRCh38 |
NC_000023.10:g.135730365C= , CM000685.1:g.135730365C= | GRCh37 |
NC_000023.9:g.135558031C= | NCBI36 |
NG_007280.1:g.5030C= , LRG_141:g.5030C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000695724.1:c.-43C= | ENSP00000512122.1:n.-43C= | |
ENST00000695725.1:c.-43C= | ENSP00000512123.1:n.-43C= | |
ENST00000695726.1:n.1C= | ||
ENST00000370629.7:c.-43C= MANE Select | ENSP00000359663.2:n.-43C= | |
ENST00000370629.6:c.-43C= | ENSP00000359663.2:n.-43C= | |
NM_000074.2:c.-43C= , LRG_141t1:c.-43C= | NP_000065.1:n.-43C= | |
NM_000074.3:c.-43C= MANE Select | NP_000065.1:n.-43C= |