HGVS | Genome Assembly |
---|---|
NC_000005.10:g.111077179C>T , CM000667.2:g.111077179C>T | GRCh38 |
NC_000005.9:g.110412877C>T , CM000667.1:g.110412877C>T | GRCh37 |
NC_000005.8:g.110440776C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344895.4:c.*1105C>T MANE Select | ENSP00000339804.3:n.*1105C>T | |
ENST00000379706.4:c.*1105C>T | ENSP00000427827.1:n.*1105C>T | |
NM_033035.4:c.*1105C>T | NP_149024.1:n.*1105C>T | |
NM_138551.4:c.*1105C>T | NP_612561.2:n.*1105C>T | |
NR_045089.1:n.2989C>T | ||
NM_033035.5:c.*1105C>T MANE Select | NP_149024.1:n.*1105C>T | |
NM_138551.5:c.*1105C>T | NP_612561.2:n.*1105C>T | |
NR_045089.2:n.3007C>T |