HGVS | Genome Assembly |
---|---|
NC_000002.12:g.176119413A= , CM000664.2:g.176119413A= | GRCh38 |
NC_000002.11:g.176984141A= , CM000664.1:g.176984141A= | GRCh37 |
NC_000002.10:g.176692387A= | NCBI36 |
NG_008133.2:g.12650A= , LRG_246:g.12650A= | |
NG_009225.1:g.1729A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000249501.5:c.*182A= MANE Select | ENSP00000249501.4:n.*182A= | |
ENST00000249501.4:c.*182A= | ENSP00000249501.4:n.*182A= | |
NM_002148.3:c.*182A= , LRG_246t1:c.*182A= | NP_002139.2:n.*182A= | |
NM_002148.4:c.*182A= MANE Select | NP_002139.2:n.*182A= |