HGVS | Genome Assembly |
---|---|
NC_000023.11:g.136659263C= , CM000685.2:g.136659263C= | GRCh38 |
NC_000023.10:g.135741422C= , CM000685.1:g.135741422C= | GRCh37 |
NC_000023.9:g.135569088C= | NCBI36 |
NG_007280.1:g.16087C= , LRG_141:g.16087C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695724.1:c.*252C= | ENSP00000512122.1:n.*252C= | |
ENST00000695725.1:c.*189C= | ENSP00000512123.1:n.*189C= | |
ENST00000695726.1:n.2602C= | ||
ENST00000695729.1:n.3437C= | ||
ENST00000370629.7:c.634C= MANE Select | ENSP00000359663.2:p.His212= | |
ENST00000370628.2:c.571C= | ENSP00000359662.2:p.His191= | |
ENST00000370629.6:c.634C= | ENSP00000359663.2:p.His212= | |
NM_000074.2:c.634C= , LRG_141t1:c.634C= | NP_000065.1:p.His212= | |
NM_000074.3:c.634C= MANE Select | NP_000065.1:p.His212= |